tag:blogger.com,1999:blog-73105455565127794222024-03-13T05:04:48.858+03:00Research group of Dmitry PerekalinDmitryhttp://www.blogger.com/profile/06591522667018423627noreply@blogger.comBlogger59125tag:blogger.com,1999:blog-7310545556512779422.post-52092323270308280152023-10-15T16:04:00.000+03:002023-10-15T16:05:53.306+03:00<p style="text-align: center;"><span style="color: #cc0000; font-family: arial; font-size: medium;"> <b>Be human, make science, not war.</b></span></p>Dmitryhttp://www.blogger.com/profile/06591522667018423627noreply@blogger.comtag:blogger.com,1999:blog-7310545556512779422.post-57552684839477425812023-10-15T16:03:00.000+03:002023-10-15T16:03:25.536+03:00<p class="MsoNormal"><span style="font-family: helvetica;"></span></p><p dir="ltr" style="line-height: 1.6; margin-bottom: 0pt; margin-top: 0pt; text-align: left;"><span style="color: #212121; font-size: 13pt; font-variant-east-asian: normal; font-variant-numeric: normal; vertical-align: baseline; white-space: pre-wrap;"><span style="font-family: arial;">We develop methods for synthesis of organic compounds of late transition metals with application in homogeneous catalysis, photochemistry, and biochemistry.</span></span></p><p class="MsoNormal"><span style="font-family: arial;"><b>Current group members</b></span></p><p class="MsoNormal"><span style="font-family: arial;"></span></p><div class="separator" style="clear: both; text-align: center;"><a href="https://blogger.googleusercontent.com/img/b/R29vZ2xl/AVvXsEgrG9t2O1ocUPSFoF2rDNckM_xvCqlBF1bRP8EZXEEVjqASO1JDlpDtjdEWUZHs4cyNUKQAa42YThNZ9PBsW57fF55GMfBORn4onheHjSPvFfgO5XjRJQ_2cZuE4YmfwI-3PiN9bqhfmXiK6Jz8zh5N51GaaqlnVMQKE7f9aBEPePijHDgKb8BLJxuGQQ/s606/curent%20members-2023.jpg" imageanchor="1" style="margin-left: 1em; margin-right: 1em;"><img border="0" data-original-height="606" data-original-width="606" height="400" src="https://blogger.googleusercontent.com/img/b/R29vZ2xl/AVvXsEgrG9t2O1ocUPSFoF2rDNckM_xvCqlBF1bRP8EZXEEVjqASO1JDlpDtjdEWUZHs4cyNUKQAa42YThNZ9PBsW57fF55GMfBORn4onheHjSPvFfgO5XjRJQ_2cZuE4YmfwI-3PiN9bqhfmXiK6Jz8zh5N51GaaqlnVMQKE7f9aBEPePijHDgKb8BLJxuGQQ/w400-h400/curent%20members-2023.jpg" width="400" /></a></div><div class="separator" style="clear: both; text-align: center;"><br /></div><p></p><h4 style="text-align: left;"><p style="text-align: left;"></p><span style="font-family: helvetica;"><p style="text-align: left;"></p><ul style="font-weight: normal; text-align: left;"><li><span><span>Prof. Dr. Dmitry S. Perekalin, Group leader, dsp@ineos.ac.ru</span></span></li></ul><ul style="font-weight: normal; text-align: left;"><li>Dr. Nikita V. Shvydkiy, researcher</li></ul><ul style="font-weight: normal; text-align: left;"><li>Dr. Roman A. Pototsky, researcher</li></ul><ul style="font-weight: normal; text-align: left;"><li>Alina A. Komarova, PhD student</li></ul><ul style="font-weight: normal; text-align: left;"><li>Nikita M. Ankudinov, PhD student</li></ul><ul style="font-weight: normal; text-align: left;"><li>Andrey M. Kolos, PhD student</li></ul><ul style="font-weight: normal; text-align: left;"><li>Mikhail A. Boym, MS student</li></ul><ul style="font-weight: normal; text-align: left;"><li>Tatiana N. Petrushina, MS student</li></ul><ul style="font-weight: normal; text-align: left;"><li><span>Dr. Evgeniya A. Trifonova, researcher (currently </span><span>on leave</span><span>)</span></li></ul><p></p></span><p></p></h4><div><div style="text-align: left;"><p dir="ltr" style="line-height: 1.6; margin-bottom: 0pt; margin-top: 0pt; text-align: center;"><span style="font-family: arial;"><span style="color: #212121; font-variant-east-asian: normal; font-variant-numeric: normal; vertical-align: baseline; white-space: pre-wrap;"></span></span></p><p dir="ltr" style="line-height: 1.6; margin-bottom: 0pt; margin-top: 0pt; text-align: center;"><span style="font-family: arial;"><span style="color: #212121; font-variant-east-asian: normal; font-variant-numeric: normal; vertical-align: baseline; white-space: pre-wrap;"></span></span></p><p dir="ltr" style="line-height: 1.6; margin-bottom: 0pt; margin-top: 0pt; text-align: center;"><span style="font-family: arial;"><span style="color: #212121; font-variant-east-asian: normal; font-variant-numeric: normal; vertical-align: baseline; white-space: pre-wrap;"></span></span></p></div><p></p><p class="MsoNormal"><b><span style="font-family: arial;"><br /></span></b></p><p class="MsoNormal"><b><span style="font-family: arial;">Former group members</span></b></p><div class="separator" style="clear: both; text-align: center;"><img border="0" data-original-height="600" data-original-width="600" height="400" src="https://1.bp.blogspot.com/-Jz8tuyzYZ2s/XzBn9acE1-I/AAAAAAAAEqc/cFSNe56MPX4SBeVSgoZwX446fvhcwQ7FACNcBGAsYHQ/w400-h400/former%2Bmembers.jpg" width="400" /></div><h4 style="text-align: left;"><ul style="text-align: left;"><li><span style="font-weight: normal;"><span style="font-family: arial;">Dr. Maria V. Babak, defended Ms thesis, left for PhD studies in the University of Vienna, Austria with Prof. Christian Hartinger</span></span></li></ul><ul style="text-align: left;"><li><span style="font-weight: normal;"><span style="font-family: arial;">Dr. Eduard E. Karslyan, defended PhD thesis, left for industrial position at BASF </span></span></li></ul><ul style="text-align: left;"><li><span style="font-weight: normal;"><span style="font-family: arial;">Dr. Andrey I. Konovalov, defended Ms thesis, left for PhD studies in ICIQ, Spain with Prof. Vladimir V. Grushin</span></span></li></ul><ul style="text-align: left;"><li><span style="font-weight: normal;"><span style="font-family: arial;">Dr. Dmitry V. Vasilyev, defended Ms thesis, left for PhD studies in EPFL, Switzerland with Prof. Paul Dyson</span></span></li></ul><ul style="text-align: left;"><li><span style="font-weight: normal;"><span style="font-family: arial;">Dr. Andrey A. Mikhailov, researcher, left for independent research in the Institute of Bioorganic Chemistry RAS</span></span></li></ul><ul style="text-align: left;"><li><span style="font-weight: normal;"><span style="font-family: arial;">Dr. Petr A. Zhmurov, researcher, left for research in Krasavin group at the Saint Petersburg State University</span></span></li></ul><ul style="text-align: left;"><li><span style="font-weight: normal;"><span style="font-family: arial;">Abdusalom A. Suleymanov, defended Ms thesis, left for PhD studies in EPFL, Switzerland with Prof. Kay Severin </span></span></li></ul><ul style="text-align: left;"><li><span style="font-weight: normal;"><span style="font-family: arial;">Natalia L. Loskutova, defended Ms thesis, left for industrial position at Mars</span></span></li></ul><ul style="text-align: left;"><li><span style="font-weight: normal;"><span style="font-family: arial;">Andrei M. Shved, defended Ms thesis, left for PhD studies in some secret place :) </span></span></li></ul></h4></div><div><div></div></div>Dmitryhttp://www.blogger.com/profile/06591522667018423627noreply@blogger.comtag:blogger.com,1999:blog-7310545556512779422.post-57687854907749699052023-10-15T16:02:00.000+03:002023-10-15T16:02:26.164+03:00<p></p><div class="separator" style="clear: both; text-align: center;"><a href="https://1.bp.blogspot.com/-lDvoQPuF7fw/XzRflx96l9I/AAAAAAAAEsc/loNlmswRSeMIPLghfcVCJlMkUrEYLOhDgCNcBGAsYHQ/s565/cover%2Bsmall.jpg" imageanchor="1" style="margin-left: 1em; margin-right: 1em;"><img border="0" data-original-height="565" data-original-width="400" src="https://1.bp.blogspot.com/-lDvoQPuF7fw/XzRflx96l9I/AAAAAAAAEsc/loNlmswRSeMIPLghfcVCJlMkUrEYLOhDgCNcBGAsYHQ/s0/cover%2Bsmall.jpg" /></a></div><span style="font-family: arial;"><br /></span><p></p><p><span style="font-family: arial;">A short textbook "Organometallic Chemistry and a bit of Catalysis" in Russian. Designed to explain organometallic chemistry to a common organic chemist. <a href="https://drive.google.com/file/d/1tWhYQKvTiq0dP3Lg3tri66caRk0dFC3l/view?usp=sharing">Download from Google Drive</a></span></p><p><span style="font-family: arial;"><br /></span></p>Dmitryhttp://www.blogger.com/profile/06591522667018423627noreply@blogger.comtag:blogger.com,1999:blog-7310545556512779422.post-74133826786815583022023-10-15T16:00:00.001+03:002023-10-15T16:00:42.859+03:00<p></p><div class="separator" style="clear: both; text-align: center;"><div class="separator" style="clear: both; text-align: center;"><a href="https://blogger.googleusercontent.com/img/b/R29vZ2xl/AVvXsEjjvRqqEcm9seUGu17xhKnT9Drqp_WV2waRz_7uS0IeVgn5zVmZHt72kxzd1hsoJ1TJSi9pxW4ZCFNcfAQDgvKBsnLyHJRDIOksFHElpQJq_fOBTPHOrmRqfZZrn5dlsB-VPKE0fJWja7rwHiR2ZPWPMx2Wob0SbGimUfaHjqLyfSiqYXTsYGwx7wmsX3tr/s986/FB.JPG" imageanchor="1" style="margin-left: 1em; margin-right: 1em;"><span style="font-family: helvetica;"><img border="0" data-original-height="497" data-original-width="986" height="281" src="https://blogger.googleusercontent.com/img/b/R29vZ2xl/AVvXsEjjvRqqEcm9seUGu17xhKnT9Drqp_WV2waRz_7uS0IeVgn5zVmZHt72kxzd1hsoJ1TJSi9pxW4ZCFNcfAQDgvKBsnLyHJRDIOksFHElpQJq_fOBTPHOrmRqfZZrn5dlsB-VPKE0fJWja7rwHiR2ZPWPMx2Wob0SbGimUfaHjqLyfSiqYXTsYGwx7wmsX3tr/w557-h281/FB.JPG" width="557" /></span></a></div><span style="font-family: helvetica;"><br /></span><div class="separator" style="clear: both; text-align: left;"><span lang="EN-US"><span style="font-family: helvetica;"><b>Photochemically induced
formation of adhesive hydrogels from sodium alginate, acrylamide, and iron
sandwich complex</b></span></span></div><div class="separator" style="clear: both; text-align: left;"><span lang="EN-US"><span style="font-family: helvetica;"><br /></span></span></div><div class="separator" style="clear: both; text-align: left;"><span style="font-family: helvetica;">A. S. Sokolov - synthesis</span></div><div class="separator" style="clear: both; text-align: left;"><span style="font-family: helvetica;">V. A.
Korabelnikova - investigation of properties</span></div><div class="separator" style="clear: both; text-align: left;"><span style="font-family: helvetica;">V. P. Ananikov - ideas, head of the lab</span></div><div class="separator" style="clear: both; text-align: left;"><span style="font-family: helvetica;">D. A. Michurov - investigation of properties</span></div><div class="separator" style="clear: both; text-align: left;"><span style="font-family: helvetica;">V. I. Lozinsky - </span><span style="font-family: helvetica;">ideas, head of the lab</span></div><div class="separator" style="clear: both; text-align: left;"><span style="font-family: helvetica;">D. S. Perekalin</span><span style="font-family: helvetica;"> - </span><span style="font-family: helvetica;">ideas, synthesis, head of the lab</span></div></div><p><span style="font-family: helvetica;"><i><span lang="EN-US">Chem</span>.
<span lang="EN-US">Commun</span>.</i> <b><span lang="EN-US">2023</span></b><span lang="EN-US">,
<i>59</i></span>, <span lang="EN-US">10532−10535</span>. <a href="https://doi.org/10.1039/D3CC03129B" target="_blank">Link</a></span></p><p></p>Dmitryhttp://www.blogger.com/profile/06591522667018423627noreply@blogger.comtag:blogger.com,1999:blog-7310545556512779422.post-9411522659910431422023-10-15T15:50:00.004+03:002023-10-15T15:54:25.332+03:00<div class="separator" style="clear: both; text-align: center;"><a href="https://blogger.googleusercontent.com/img/a/AVvXsEimIH1cREKyLRRF-x9y-RysqnPn08iAHrRaOkoMHxYUbGhgWH_5HT2abYlJWzlMq3uFPc8S0dhNEd23oxBkzsFpFWbmt3Iae6l6GLK4pfs48QDCLrfUwwDl0lFkvgf6ZUja-sq4WfmBrqUPGuW7ITJ2mCTwvj02SnI3MUzpwSouISripRZPhxC-QGP9ulcI" style="margin-left: 1em; margin-right: 1em; text-align: center;"><img data-original-height="424" data-original-width="674" height="251" src="https://blogger.googleusercontent.com/img/a/AVvXsEimIH1cREKyLRRF-x9y-RysqnPn08iAHrRaOkoMHxYUbGhgWH_5HT2abYlJWzlMq3uFPc8S0dhNEd23oxBkzsFpFWbmt3Iae6l6GLK4pfs48QDCLrfUwwDl0lFkvgf6ZUja-sq4WfmBrqUPGuW7ITJ2mCTwvj02SnI3MUzpwSouISripRZPhxC-QGP9ulcI=w400-h251" width="400" /></a></div><p><b><span style="font-family: helvetica;">Noble metal versus abundant metal catalysts in fine organic synthesis: cost comparison of C−H activation
methods</span></b></p><div class="separator" style="clear: both; text-align: left;"><span lang="EN-US"><span style="background-color: white; color: #494949;"><span style="font-family: helvetica;">A. A. Komarova - calculations</span></span></span></div><div class="separator" style="clear: both; text-align: left;"><span lang="EN-US"><span style="background-color: white; color: #494949;"><span style="font-family: helvetica;">D. S. Perekalin - ideas, head of the lab</span></span></span></div><div class="separator" style="clear: both; text-align: left;"><span lang="EN-US"><span style="background-color: white; color: #494949;"><span style="font-family: helvetica;"><br /></span></span></span></div><div class="separator" style="clear: both; text-align: left;"><span lang="EN-US"><span style="font-family: helvetica;"><i><span lang="EN-US">Organometallics</span></i><span lang="EN-US">
<b>2023</b>, 42, 1433−1438. <a href="https://pubs.acs.org/doi/10.1021/acs.organomet.3c00153" target="_blank">Link</a></span></span></span></div><p></p>Dmitryhttp://www.blogger.com/profile/06591522667018423627noreply@blogger.comtag:blogger.com,1999:blog-7310545556512779422.post-8202276240132013682022-12-02T15:34:00.000+03:002023-02-23T15:38:52.664+03:00<p><b style="font-family: helvetica;"></b></p><div class="separator" style="clear: both; text-align: center;"><div class="separator" style="clear: both; text-align: center;"><b style="font-family: helvetica;"><a href="https://blogger.googleusercontent.com/img/b/R29vZ2xl/AVvXsEgKqBvArgE0kB_1wxNCkC1eczJiS_r87UVn3IpAdH8KKeWl50WCHUvkJsuLgfWeb8EnQ2UiYLpFclQNtlZbqKH0RD8FnK24FLV_llmVLmdl43bDNG2bPZCUzNwtJqS17jP6tO64IcyPcsIXWqGrEa7N2ZyTZWR2uUK1n0iag8VJ7Ce2doomfnF6eWcMqg/s1274/99.GIF" style="margin-left: 1em; margin-right: 1em;"><img border="0" data-original-height="725" data-original-width="1274" height="228" src="https://blogger.googleusercontent.com/img/b/R29vZ2xl/AVvXsEgKqBvArgE0kB_1wxNCkC1eczJiS_r87UVn3IpAdH8KKeWl50WCHUvkJsuLgfWeb8EnQ2UiYLpFclQNtlZbqKH0RD8FnK24FLV_llmVLmdl43bDNG2bPZCUzNwtJqS17jP6tO64IcyPcsIXWqGrEa7N2ZyTZWR2uUK1n0iag8VJ7Ce2doomfnF6eWcMqg/w400-h228/99.GIF" width="400" /></a></b></div><b style="font-family: helvetica;"><div class="separator" style="clear: both; text-align: center;"><br /></div></b></div><p></p><p><b style="font-family: helvetica;">Cyclobutadiene platinum complex as a new type of precatalyst for hydrosilylation of alkenes and alkynes</b></p><p></p><p></p><div><span lang="EN-US" style="font-size: 12pt;"><span style="font-family: helvetica;">N. V. Shvydkiy - synthesis, ideas<br /></span></span><span lang="EN-US" style="font-size: 12pt;"><span style="font-family: helvetica;">K. V. Rimskiy - catalytic reactions<br /></span></span><span lang="EN-US" style="font-size: 12pt;"><span style="font-family: helvetica;">D. S. Perekalin - ideas, head of the lab</span></span></div><p><span lang="EN-US" style="font-size: 12pt;"><span style="font-family: helvetica;"><i><span style="font-size: 12pt;">Appl. Organomet. Chem.</span></i><span style="font-size: 12pt;"> <b>2</b></span><b><span lang="EN-US" style="font-size: 12pt;">023</span></b><span lang="EN-US" style="font-size: 12pt;">, <i>37</i>, e7008. <a href="https://doi.org/10.1002/aoc.7008">Link</a></span></span></span></p>Dmitryhttp://www.blogger.com/profile/06591522667018423627noreply@blogger.comtag:blogger.com,1999:blog-7310545556512779422.post-47376513649960803292022-12-01T13:45:00.001+03:002022-12-04T13:50:29.964+03:00<p></p><div class="separator" style="clear: both; text-align: center;"><a href="https://blogger.googleusercontent.com/img/b/R29vZ2xl/AVvXsEg_ieyfyYAKvObJun9MibQgsJ9q0SzJ82smdzUpYjSvfDCpK-Kw_GMY36138nESriyqi3SuhL3c_kUCHLilzEhjV0pz0kGZLUGWOSuY4x-J-WzpDEOd8fy6PZ4F6obfwDRSiwFZ7ZWb-KDUTFf39pe2SkgvnF0f5Lo1ki88iTq7gr0o47H-PmaMiiAxoA/s500/98.gif" imageanchor="1" style="margin-left: 1em; margin-right: 1em;"><img border="0" data-original-height="231" data-original-width="500" height="185" src="https://blogger.googleusercontent.com/img/b/R29vZ2xl/AVvXsEg_ieyfyYAKvObJun9MibQgsJ9q0SzJ82smdzUpYjSvfDCpK-Kw_GMY36138nESriyqi3SuhL3c_kUCHLilzEhjV0pz0kGZLUGWOSuY4x-J-WzpDEOd8fy6PZ4F6obfwDRSiwFZ7ZWb-KDUTFf39pe2SkgvnF0f5Lo1ki88iTq7gr0o47H-PmaMiiAxoA/w400-h185/98.gif" width="400" /></a></div><b style="font-family: helvetica; font-size: 12pt;"><div><b style="font-family: helvetica; font-size: 12pt;"><br /></b></div></b><span style="font-family: helvetica;"><b>Catalytic and Stoichiometric Reactions of the Parent Olefin Rhodium(I) Complex with Alkynes</b></span><p></p><p></p><div><span lang="EN-US" style="font-size: 12pt;"><span style="font-family: helvetica;">А. М. Kolos - synthesis<br /></span></span><span lang="EN-US" style="font-size: 12pt;"><span style="font-family: helvetica;">Y. V. Nelyubina - X-ray<br /></span></span><span lang="EN-US" style="font-size: 12pt;"><span style="font-family: helvetica;">D. S. Perekalin - idea, head of the lab</span></span></div><p><span lang="EN-US" style="font-size: 12pt;"><span style="font-family: helvetica;"><i><span style="font-size: 12pt;">Organometallics</span></i><span style="font-size: 12pt;"> <b>2</b></span><b><span lang="EN-US" style="font-size: 12pt;">022</span></b><span lang="EN-US" style="font-size: 12pt;">, <i>41</i>, 3038-3043. <a href="https://doi.org/10.1021/acs.organomet.2c00456">Link</a></span></span></span></p>Dmitryhttp://www.blogger.com/profile/06591522667018423627noreply@blogger.comtag:blogger.com,1999:blog-7310545556512779422.post-67336413146737327062022-08-25T18:54:00.005+03:002022-08-25T18:54:54.815+03:00<p> </p><div class="separator" style="clear: both; text-align: center;"><a href="https://blogger.googleusercontent.com/img/b/R29vZ2xl/AVvXsEhwjGyD-yLJ0CAcrJ3bI3qBlogh47Q4AI6Kq1OWF1qOhinczXDXc_Nx39rhCSPVc0le9MZAJQCAgvN62qMZwO_mpuw2DI_3Tm517HMdpppodX2aif1QSMtNOYcWbOnulnMEO7Nqoo22YVII7J48EkcE7epD-L2uDb_u5BGebHixlzmA5bGal--N7qEIEw/s964/97.gif" imageanchor="1" style="margin-left: 1em; margin-right: 1em;"><img border="0" data-original-height="964" data-original-width="787" height="320" src="https://blogger.googleusercontent.com/img/b/R29vZ2xl/AVvXsEhwjGyD-yLJ0CAcrJ3bI3qBlogh47Q4AI6Kq1OWF1qOhinczXDXc_Nx39rhCSPVc0le9MZAJQCAgvN62qMZwO_mpuw2DI_3Tm517HMdpppodX2aif1QSMtNOYcWbOnulnMEO7Nqoo22YVII7J48EkcE7epD-L2uDb_u5BGebHixlzmA5bGal--N7qEIEw/s320/97.gif" width="261" /></a></div><div class="separator" style="clear: both; text-align: center;"><br /></div><span lang="EN-US" style="font-size: 12pt;"><span style="font-family: helvetica;"><b>Synthesis of the sterically
shielded rhodium(I) arene complex by cycloaddition of the phosphorous-substituted
alkyne</b></span></span><p></p><div style="text-align: left;"><span lang="EN-US" style="font-size: 12pt;"><span style="font-family: helvetica;">R. A. Pototskiy - synthesis<br /></span></span><span lang="EN-US" style="font-size: 12pt;"><span style="font-family: helvetica;">M. A.
Boym - synthesis<br /></span></span><span lang="EN-US" style="font-size: 12pt;"><span style="font-family: helvetica;">Y. V. Nelyubina - X-ray<br /></span></span><span lang="EN-US" style="font-size: 12pt;"><span style="font-family: helvetica;">D. S. Perekalin - DFT calculations, head of the lab</span></span></div><p><span lang="EN-US" style="font-size: 12pt;"><span style="font-family: helvetica;"><i><span lang="EN-US" style="font-size: 12pt;">Z</span><span style="font-size: 12pt;">. </span><span lang="EN-US" style="font-size: 12pt;">Anorg</span><span style="font-size: 12pt;">. </span><span lang="EN-US" style="font-size: 12pt;">Allg</span><span style="font-size: 12pt;">. </span><span lang="EN-US" style="font-size: 12pt;">Chem</span><span style="font-size: 12pt;">.</span></i><span style="font-size: 12pt;"> <b>2</b></span><b><span lang="EN-US" style="font-size: 12pt;">022</span></b><span lang="EN-US" style="font-size: 12pt;">, e202200231. <a href="http://doi.org/10.1002/zaac.202200231">Link</a></span></span></span></p>Dmitryhttp://www.blogger.com/profile/06591522667018423627noreply@blogger.comtag:blogger.com,1999:blog-7310545556512779422.post-54356518454207856612022-08-25T18:49:00.003+03:002022-08-25T18:49:26.806+03:00<p> </p><div class="separator" style="clear: both; text-align: center;"><a href="https://blogger.googleusercontent.com/img/b/R29vZ2xl/AVvXsEicCw5X-y0kpF0BcyDXh_Zm2VrtikVN7W_IhuI6RO55nkBuitg2yHCyphwmYGVEdmCNrz3Eiwp8KTmW10o3EYrmFU7yneD9-ccWTs421q3S4kwYKPtyP65N202PwPe-PhhXfIAzHBNEdPLarJLpOqlnXv7Kgv6YV7fJjnR5nGxSlcV0R2SUTYPydoLAqw/s1102/96.gif" imageanchor="1" style="margin-left: 1em; margin-right: 1em;"><img border="0" data-original-height="504" data-original-width="1102" height="183" src="https://blogger.googleusercontent.com/img/b/R29vZ2xl/AVvXsEicCw5X-y0kpF0BcyDXh_Zm2VrtikVN7W_IhuI6RO55nkBuitg2yHCyphwmYGVEdmCNrz3Eiwp8KTmW10o3EYrmFU7yneD9-ccWTs421q3S4kwYKPtyP65N202PwPe-PhhXfIAzHBNEdPLarJLpOqlnXv7Kgv6YV7fJjnR5nGxSlcV0R2SUTYPydoLAqw/w400-h183/96.gif" width="400" /></a></div><span lang="EN-US" style="font-size: 12pt;"><span style="font-family: helvetica;"><b>Cyclopentadienyl
rhodium(III) complexes as catalysts for the insertion of phenyldiazoacetate
into E−H bonds</b></span></span><p></p><div style="text-align: left;"><span lang="EN-US" style="font-size: 12pt;"><span style="font-family: helvetica;">A. A. Komarova - synthesis<br /></span></span><span lang="EN-US" style="font-size: 12pt;"><span style="font-family: helvetica;">D. V.
Muratov - NMR<br /></span></span><span lang="EN-US" style="font-size: 12pt;"><span style="font-family: helvetica;">D. S. Perekalin - head of the lab</span></span></div><p><span lang="EN-US" style="font-size: 12pt;"><span style="font-family: helvetica;"><i><span lang="EN-US" style="font-size: 12pt;">Mend</span><span style="font-size: 12pt;">. </span><span lang="EN-US" style="font-size: 12pt;">Commun</span><span style="font-size: 12pt;">.</span></i><span style="font-size: 12pt;"> </span><b><span lang="EN-US" style="font-size: 12pt;">2022</span></b><span lang="EN-US" style="font-size: 12pt;">, <i>32</i>, 482−484. <a href="http://doi.org/10.1016/j.mencom.2022.07.017">Link</a></span></span></span></p>Dmitryhttp://www.blogger.com/profile/06591522667018423627noreply@blogger.comtag:blogger.com,1999:blog-7310545556512779422.post-26919155211861834822022-08-25T18:34:00.002+03:002022-08-25T18:34:20.469+03:00<p style="text-align: left;"></p><p style="clear: both; text-align: center;"><a href="https://blogger.googleusercontent.com/img/b/R29vZ2xl/AVvXsEgC-4T5Z2VNB5gaHG7HSh3s_gMVNqIcJ-s4GJnLx_pOuQINBi-hQynmpqW2z8-DEZ83BTgdqEdHqBSj1m2-6keyF8fFVWCUrgkasHUHS3R1g_6jFZdF_Ai4jEh9brPK_h6KVPhzukHxhEeElvPj0waQ9RMEOhIqHLEB9RCHbSWsVUXauY-MAkcGRxdh_A/s1181/95.gif" imageanchor="1" style="margin-left: 1em; margin-right: 1em;"><img border="0" data-original-height="544" data-original-width="1181" height="184" src="https://blogger.googleusercontent.com/img/b/R29vZ2xl/AVvXsEgC-4T5Z2VNB5gaHG7HSh3s_gMVNqIcJ-s4GJnLx_pOuQINBi-hQynmpqW2z8-DEZ83BTgdqEdHqBSj1m2-6keyF8fFVWCUrgkasHUHS3R1g_6jFZdF_Ai4jEh9brPK_h6KVPhzukHxhEeElvPj0waQ9RMEOhIqHLEB9RCHbSWsVUXauY-MAkcGRxdh_A/w400-h184/95.gif" width="400" /></a></p><b style="font-family: helvetica; font-size: 12pt;">Asymmetric
cyclopropanation of electron-rich alkenes by the racemic diene rhodium
catalyst: the chiral poisoning approach</b><p></p><div style="text-align: left;"><span lang="EN-US" style="font-size: 12pt;"><span style="font-family: helvetica;">E. A. Trifonova - synthesis<br /></span></span><span lang="EN-US" style="font-size: 12pt;"><span style="font-family: helvetica;">N. M.
Ankudinov - synthesis, DFT<br /></span></span><span lang="EN-US" style="font-size: 12pt;"><span style="font-family: helvetica;">D. A. Chusov - ideas, HPLC<br /></span></span><span lang="EN-US" style="font-size: 12pt;"><span style="font-family: helvetica;">Y. V. Nelyubina - X-ray<br /></span></span><span lang="EN-US" style="font-size: 12pt;"><span style="font-family: helvetica;">D. S. Perekalin - concept, a bit of DFT, head of the lab</span></span></div><p><span lang="EN-US" style="font-size: 12pt;"><span style="font-family: helvetica;"><i><span lang="EN-US" style="font-size: 12pt;">Chem</span><span style="font-size: 12pt;">. </span><span lang="EN-US" style="font-size: 12pt;">Commun</span><span style="font-size: 12pt;">.</span></i><span style="font-size: 12pt;"> </span><b><span lang="EN-US" style="font-size: 12pt;">2022</span></b><span lang="EN-US" style="font-size: 12pt;">, <i>58</i></span><span style="font-size: 12pt;">, 6709−6712. <a href="https://doi.org/10.1039/D2CC01648F">Link</a></span></span></span></p>Dmitryhttp://www.blogger.com/profile/06591522667018423627noreply@blogger.comtag:blogger.com,1999:blog-7310545556512779422.post-8782415625520559562022-08-25T17:55:00.004+03:002022-08-25T17:55:52.923+03:00<p> </p><div class="separator" style="clear: both; text-align: center;"><a href="https://blogger.googleusercontent.com/img/b/R29vZ2xl/AVvXsEicBhR9nA_S0gD_WgUo-Cxxh2Qs0b3kzCIkcG2VY0zdAg4ARqWU4LnOI5In62yGYBXlUTVNQjJfIDOXpYU3bj481jG7lCpq6EitDfedajajlm56SXBFAeciAutbezUwNMvvfrERSmyBQeppDerPMEf1qFnHdQT8ULNq4G8M9v1Vse2lhadoycd7GOj9uA/s1024/94.gif" imageanchor="1" style="margin-left: 1em; margin-right: 1em;"><img border="0" data-original-height="264" data-original-width="1024" height="128" src="https://blogger.googleusercontent.com/img/b/R29vZ2xl/AVvXsEicBhR9nA_S0gD_WgUo-Cxxh2Qs0b3kzCIkcG2VY0zdAg4ARqWU4LnOI5In62yGYBXlUTVNQjJfIDOXpYU3bj481jG7lCpq6EitDfedajajlm56SXBFAeciAutbezUwNMvvfrERSmyBQeppDerPMEf1qFnHdQT8ULNq4G8M9v1Vse2lhadoycd7GOj9uA/w494-h128/94.gif" width="494" /></a></div><span lang="EN-US" style="font-size: 12pt;"><span style="font-family: helvetica;"><p><span style="font-size: 12pt;"><b>Generation of
cyclopentadiene for Diels-Alder reactions by visible-light irradiation of iron
sandwich complexes</b></span></p><div style="text-align: left;"><span lang="EN-US" style="font-size: 12pt;">A. S. Sokolov - synthesis<br /></span><span lang="EN-US" style="font-size: 12pt;">A. V.
Polezhaev - idea<br /></span><span lang="EN-US" style="font-size: 12pt;">Y. V. Nelyubina - X-ray<br /></span><span lang="EN-US" style="font-size: 12pt;">D. S. Perekalin - a bit of synthesis, head of the lab</span></div><p><span lang="EN-US" style="font-size: 12pt;"><i><span lang="EN-US" style="font-size: 12pt;">Helv. Chim. Acta</span></i><span lang="EN-US" style="font-size: 12pt;"> <b>2022</b>, <i>105</i>, e202100246. <a href="https://doi.org/10.1002/hlca.202100246">Link</a></span></span></p></span></span><p></p>Dmitryhttp://www.blogger.com/profile/06591522667018423627noreply@blogger.comtag:blogger.com,1999:blog-7310545556512779422.post-24722547190908529082022-08-25T16:58:00.003+03:002023-02-23T15:25:52.250+03:00<p> </p><div class="separator" style="clear: both; text-align: center;"><a href="https://blogger.googleusercontent.com/img/b/R29vZ2xl/AVvXsEj566ILfHXetnxtCLfgSmttuE04LVD1XNrFf120jzJgwE_OK-Ixu_6T_RD5Bpo0plmpmDDMJ_65rdhhHaVbCGFt8YaK5hJnsMDc1F-iAjb8Dp9Mc-o7-wPZrPsXexv9aU78W9X5X_QUjUAk5m009Ja5z73cQF7G5b1Cx4uCRfGePMJuNL7r7G1JzcDNYg/s945/93.gif" style="margin-left: 1em; margin-right: 1em;"><img border="0" data-original-height="415" data-original-width="945" height="248" src="https://blogger.googleusercontent.com/img/b/R29vZ2xl/AVvXsEj566ILfHXetnxtCLfgSmttuE04LVD1XNrFf120jzJgwE_OK-Ixu_6T_RD5Bpo0plmpmDDMJ_65rdhhHaVbCGFt8YaK5hJnsMDc1F-iAjb8Dp9Mc-o7-wPZrPsXexv9aU78W9X5X_QUjUAk5m009Ja5z73cQF7G5b1Cx4uCRfGePMJuNL7r7G1JzcDNYg/w563-h248/93.gif" width="563" /></a></div><div class="separator" style="clear: both; text-align: center;"><br /></div><p></p><p><span lang="EN-US" style="font-size: 12pt;"><span style="font-family: helvetica;"><b>Synthesis of ruthenium
catalysts with chiral arene ligand derived from natural camphor.</b></span></span></p><div style="text-align: left;"><span style="font-family: helvetica;"><span lang="EN-US" style="font-size: 12pt;">R. A. Pototskiy - synthesis, ideas<br /></span><span lang="EN-US" style="font-size: 12pt;">M. A.
Boym - synthesis<br /></span><span lang="EN-US" style="font-size: 12pt;">Y. V. Nelyubina - X-ray<br /></span><span lang="EN-US" style="font-size: 12pt;">D. S. Perekalin - ideas, DFT calculations, head of the lab</span></span></div><p><span lang="EN-US" style="font-size: 12pt;"><span style="font-family: helvetica;"><i><span lang="EN-US" style="font-size: 12pt;">Synthesis</span></i><span lang="EN-US" style="font-size: 12pt;"> <b>2022</b>, <i>54</i>,</span></span></span><span style="font-family: arial;"> 4721-4726<span style="font-size: 12pt;">.</span></span><span style="font-family: helvetica; font-size: 12pt;"> </span><a href="https://doi.org/10.1055/a-1668-2075" style="font-family: helvetica; font-size: 12pt;">Link</a></p>Dmitryhttp://www.blogger.com/profile/06591522667018423627noreply@blogger.comtag:blogger.com,1999:blog-7310545556512779422.post-23002466475598898212022-08-25T15:51:00.004+03:002022-08-25T15:53:46.290+03:00<div class="separator" style="clear: both; text-align: center;"><span style="color: #444444; font-family: helvetica;"><a href="https://blogger.googleusercontent.com/img/b/R29vZ2xl/AVvXsEhVrqJFDqU5swF3GKKDzo2sKyEE63JEyy3azBIQ8zC--Rby6MUP5oQpNLnCThxHbKI9m4KQDQ3jteOnS3suqDk6LX9yb1V63_SbPwmbUFOeoigYwUgcfbMMIei2hzrATYwlXfYLYi3WmNCRqFQiywOoNmnBOB1sy6-MmQXhRfAR_-zxU4_TJgxumZKRYw/s2728/92.jpg" style="margin-left: 1em; margin-right: 1em;"><img border="0" data-original-height="760" data-original-width="2728" height="156" src="https://blogger.googleusercontent.com/img/b/R29vZ2xl/AVvXsEhVrqJFDqU5swF3GKKDzo2sKyEE63JEyy3azBIQ8zC--Rby6MUP5oQpNLnCThxHbKI9m4KQDQ3jteOnS3suqDk6LX9yb1V63_SbPwmbUFOeoigYwUgcfbMMIei2hzrATYwlXfYLYi3WmNCRqFQiywOoNmnBOB1sy6-MmQXhRfAR_-zxU4_TJgxumZKRYw/w560-h156/92.jpg" width="560" /></a></span></div><span style="color: #444444; font-family: helvetica;"><br /><div class="separator" style="clear: both; text-align: center;"><a href="https://blogger.googleusercontent.com/img/b/R29vZ2xl/AVvXsEiGxX0726y7iWbY4l75u9CPwivr51bqfc_yTUp3DWCDjPBjPvtYYtv_ilV9Kk7mRbsZKhwPsCqNu8ERJY2b6uYoftwQ_tScIQxvF-R94_j9VWHhTEd4TGNMTeZ7wUUEglPbr2zoobzBhIAncVigfq-1fP5rvhDvZxUS3yRZQ0EIBBmXejmf3vGYSLr-JQ/s1659/92-cover.jpg" style="font-size: 12pt; margin-left: 1em; margin-right: 1em;"><img border="0" data-original-height="1659" data-original-width="1251" height="320" src="https://blogger.googleusercontent.com/img/b/R29vZ2xl/AVvXsEiGxX0726y7iWbY4l75u9CPwivr51bqfc_yTUp3DWCDjPBjPvtYYtv_ilV9Kk7mRbsZKhwPsCqNu8ERJY2b6uYoftwQ_tScIQxvF-R94_j9VWHhTEd4TGNMTeZ7wUUEglPbr2zoobzBhIAncVigfq-1fP5rvhDvZxUS3yRZQ0EIBBmXejmf3vGYSLr-JQ/s320/92-cover.jpg" width="241" /></a></div></span><div style="text-align: left;"><span style="font-size: 12pt;"><span style="color: #444444; font-family: helvetica;"><br /></span></span></div><p style="text-align: left;"><span style="color: #444444; font-family: helvetica;"><span style="font-size: 12pt;"><b style="color: black; font-family: "Times New Roman";"><span style="color: #444444; font-family: helvetica;">Planar chiral rhodium complexes of 1,4-benzoquinones</span></b></span></span></p><div style="text-align: left;"><span style="color: #444444; font-family: helvetica;"><span style="font-size: 12pt;">N. M. Ankudinov - synthesis, DFT<br /></span><span lang="EN-US" style="font-size: 12pt;">Y. V.
Nelyubina - X-ray<br /></span><span lang="EN-US" style="font-size: 12pt;">D. S. Perekalin - ideas, DFT, head of the lab<br /></span><span lang="EN-US" style="font-size: 12pt;">special thanks to Maria Pikunova for Cover design</span></span></div><p></p><p><span lang="EN-US" style="font-size: 12pt;"><span style="color: #444444; font-family: helvetica;"><i><span lang="EN-US" style="font-size: 12pt;">Chem. Eur. J.</span></i><span lang="EN-US" style="font-size: 12pt;"> <b>2022</b>, <i>28</i>, e202200195. <a href="http://doi.org/10.1002/chem.202200195">Link</a></span></span></span></p>Dmitryhttp://www.blogger.com/profile/06591522667018423627noreply@blogger.comtag:blogger.com,1999:blog-7310545556512779422.post-56052488088792629432022-08-25T15:32:00.001+03:002022-08-25T16:01:11.195+03:00<p><br /></p><div class="separator" style="clear: both; text-align: center;"><a href="https://blogger.googleusercontent.com/img/b/R29vZ2xl/AVvXsEik2yzjaErQaWPcn8vkZprFr1b3Y95J7HwPmD7UFItfMg6WgHWiTqnTa7ISpr_acEBQEKfeaLriqK9I3ho06ETaQjO_33B9fRUIirj84Q8AMnUQqavzOw7nh-4-XGdYghbljRUehecQNijxd4DEY_fAbBZoTn9yiXFVglE8x737ThcuQbXw1uNejCTyEw/s500/90-2.gif" style="margin-left: 1em; margin-right: 1em;"><img border="0" data-original-height="193" data-original-width="500" height="155" src="https://blogger.googleusercontent.com/img/b/R29vZ2xl/AVvXsEik2yzjaErQaWPcn8vkZprFr1b3Y95J7HwPmD7UFItfMg6WgHWiTqnTa7ISpr_acEBQEKfeaLriqK9I3ho06ETaQjO_33B9fRUIirj84Q8AMnUQqavzOw7nh-4-XGdYghbljRUehecQNijxd4DEY_fAbBZoTn9yiXFVglE8x737ThcuQbXw1uNejCTyEw/w400-h155/90-2.gif" width="400" /></a></div><div class="separator" style="clear: both; text-align: center;"><div class="separator" style="clear: both; text-align: center;"><br /></div><div class="separator" style="clear: both; text-align: center;"><a href="https://blogger.googleusercontent.com/img/b/R29vZ2xl/AVvXsEhrQIg9n2G0bs_or90KdPH1rBloqYbArMgaY6nX39TOQqC8m5Kqejn-jAE63RQbgz4zmqpIRclkNG1TCn1htAhjwXTNYLpAVLiKXQC5fX3djRHfJK3NdIeVv_EICZqpEUz1s_RmbbOgYjBsKaEuvnWQmZqZi-CP86ptkHzP8ZlQtd2XzgxUZMHgusTBrw/s768/91-cover.jpg" imageanchor="1" style="margin-left: 1em; margin-right: 1em;"><img border="0" data-original-height="768" data-original-width="578" height="320" src="https://blogger.googleusercontent.com/img/b/R29vZ2xl/AVvXsEhrQIg9n2G0bs_or90KdPH1rBloqYbArMgaY6nX39TOQqC8m5Kqejn-jAE63RQbgz4zmqpIRclkNG1TCn1htAhjwXTNYLpAVLiKXQC5fX3djRHfJK3NdIeVv_EICZqpEUz1s_RmbbOgYjBsKaEuvnWQmZqZi-CP86ptkHzP8ZlQtd2XzgxUZMHgusTBrw/s320/91-cover.jpg" width="241" /></a></div><br /><div class="separator" style="clear: both; text-align: center;"><br /></div></div><span lang="EN-US" style="font-size: 12pt;"><span style="color: #444444; font-family: helvetica;"><b>Synthesis of overloaded
cyclopentadienyl rhodium(III) complexes via cyclotetramerization of
tert-butylacetylene</b></span></span><p></p><div style="text-align: left;"><span lang="EN-US" style="font-size: 12pt;"><span style="color: #444444; font-family: helvetica;">A. V. Kolos - synthesis<br /></span></span><span lang="EN-US" style="font-size: 12pt;"><span style="color: #444444; font-family: helvetica;">Y. V.
Nelyubina - X-ray<br /></span></span><span lang="EN-US" style="font-size: 12pt;"><span style="color: #444444; font-family: helvetica;">B. Sundararaju - advice<br /></span></span><span style="color: #444444;"><span lang="EN-US" style="font-size: 12pt;"><span style="font-family: helvetica;">D. S. Perekalin - ideas, </span></span><span style="background-color: white; font-family: arial; font-size: 14.85px;">DFT, head of the lab</span></span></div><p><span lang="EN-US" style="font-size: 12pt;"><span style="color: #444444; font-family: helvetica;"><i><span lang="EN-US" style="font-size: 12pt;">Organometallics</span></i><span lang="EN-US" style="font-size: 12pt;"> <b>2021</b>, <i>40</i>, 3712−3719. <a href="https://doi.org/10.1021/acs.organomet.1c00403" target="_blank">Link</a></span></span></span></p>Dmitryhttp://www.blogger.com/profile/06591522667018423627noreply@blogger.comtag:blogger.com,1999:blog-7310545556512779422.post-42874121909175356992021-07-13T04:05:00.003+03:002022-08-25T14:53:53.316+03:00<p> </p><div class="separator" style="clear: both; text-align: center;"><a href="https://1.bp.blogspot.com/-fLFXKDfpSDg/YOzmJc3mCLI/AAAAAAAAFdU/VAUCX0scHfk8z-jG9-kdqu3JOQ1xhqGgwCNcBGAsYHQ/s700/90.gif" style="margin-left: 1em; margin-right: 1em;"><img border="0" data-original-height="311" data-original-width="700" height="189" src="https://1.bp.blogspot.com/-fLFXKDfpSDg/YOzmJc3mCLI/AAAAAAAAFdU/VAUCX0scHfk8z-jG9-kdqu3JOQ1xhqGgwCNcBGAsYHQ/w425-h189/90.gif" width="425" /></a></div><p></p><p><b style="color: #494949; font-family: arial; font-size: 14.85px;">Synthesis of rhodium complexes with chiral diene ligands via diastereoselective coordination and their application in the asymmetric insertion of diazo compounds into E-H bonds</b></p><p></p><p></p><p style="background-color: white; color: #494949; font-family: arial, tahoma, helvetica, freesans, sans-serif; font-size: 14.85px;"><span style="font-family: arial;"><span lang="">N</span>. <span lang="">M</span>. Ankudinov<span lang=""> - a lot of synthesis, DFT calculations, many ideas<br />D. A. Chusov - HPLC, some ideas<br />Y. V. Nelyubina - X-ray<br /></span><span lang=""><span face=""><span lang=""><span face="">D. S. Perekalin - concept, DFT calculations, head of the lab<br /><span face=""><span lang=""><i><span lang=""><br /></span></i></span></span></span></span></span></span></span></p><p><span style="background-color: white; color: #494949; font-family: arial; font-size: 14.85px;"><i><span lang="">Angew. Chem. Int. Ed.</span></i><span lang="">, <b>2021</b>, <i>60</i>, 18712-18720.</span> </span><a href="https://doi.org/10.1002/anie.202105179" style="background-color: white; color: #00669b; font-family: arial; font-size: 14.85px; text-decoration-line: none;" target="_blank">Link</a> </p>Dmitryhttp://www.blogger.com/profile/06591522667018423627noreply@blogger.comtag:blogger.com,1999:blog-7310545556512779422.post-60260358427368948962021-07-13T04:01:00.001+03:002021-07-13T04:01:44.268+03:00<p> </p><div class="separator" style="clear: both; text-align: center;"><a href="https://1.bp.blogspot.com/-_qEC5PVHC3w/YOzlOzyVpfI/AAAAAAAAFdM/cBrSEMUxdsQikTvpaOEgIgEMwb0-kdA0gCNcBGAsYHQ/s1181/for%2BFB.jpg" style="margin-left: 1em; margin-right: 1em;"><img border="0" data-original-height="678" data-original-width="1181" height="286" src="https://1.bp.blogspot.com/-_qEC5PVHC3w/YOzlOzyVpfI/AAAAAAAAFdM/cBrSEMUxdsQikTvpaOEgIgEMwb0-kdA0gCNcBGAsYHQ/w497-h286/for%2BFB.jpg" width="497" /></a></div><p></p><p><b style="color: #494949; font-family: arial; font-size: 14.85px;">Cyclobutadiene rhodium complexes as catalysts for the synthesis of amides from electron-rich arenes, tosyl azide and CO</b></p><p></p><p></p><p style="background-color: white; color: #494949; font-family: arial, tahoma, helvetica, freesans, sans-serif; font-size: 14.85px;"><span style="font-family: arial;"><span lang="">N</span>. <span lang="">V</span>. Shvydkiy<span lang=""> - synthesis<br />T. N. Petrushina - synthesis<br /></span><span lang=""><span face=""><span lang=""><span face="">D. S. Perekalin - DFT, head of the lab<br /><span face=""><span lang=""><i><span lang=""><br /></span></i></span></span></span></span></span></span></span></p><p><span style="background-color: white; color: #494949; font-family: arial; font-size: 14.85px;"><i><span lang="">ChemCatChem</span></i><span lang="">, <b>2021</b>, <i>13</i>,<i></i> 2873-2878.</span> </span><a href="https://doi.org/10.1002/cctc.202100344" style="background-color: white; color: #00669b; font-family: arial; font-size: 14.85px; text-decoration-line: none;" target="_blank">Link</a> </p>Dmitryhttp://www.blogger.com/profile/06591522667018423627noreply@blogger.comtag:blogger.com,1999:blog-7310545556512779422.post-36164073551204116872021-07-13T03:57:00.000+03:002021-07-13T03:56:59.985+03:00<div class="separator" style="clear: both; text-align: center;"><a href="https://1.bp.blogspot.com/-zTiIX_cK-J8/YOzj-1HCisI/AAAAAAAAFdE/AFNJ9KzKCP4Y58iBvSXOud_vJOuSpxJNwCNcBGAsYHQ/s800/87.gif" style="margin-left: 1em; margin-right: 1em;"><img border="0" data-original-height="383" data-original-width="800" height="252" src="https://1.bp.blogspot.com/-zTiIX_cK-J8/YOzj-1HCisI/AAAAAAAAFdE/AFNJ9KzKCP4Y58iBvSXOud_vJOuSpxJNwCNcBGAsYHQ/w527-h252/87.gif" width="527" /></a></div><p><b style="color: #494949; font-family: arial; font-size: 14.85px;">Synthesis of catalytically active diene and cyclopentadienyl rhodium halide complexes</b></p><p></p><p></p><p style="background-color: white; color: #494949; font-family: arial, tahoma, helvetica, freesans, sans-serif; font-size: 14.85px;"><span style="font-family: arial;"><span lang="">A</span>. <span lang="">V</span>. Kolos<span lang=""> - review<br /></span><span lang=""><span face=""><span lang=""><span face="">D. S. Perekalin - review, head of the lab<br /><span face=""><span lang=""><i><span lang=""><br /></span></i></span></span></span></span></span></span></span></p><p><span style="background-color: white; color: #494949; font-family: arial; font-size: 14.85px;"><i><span lang="">Mendeleev Commun.</span></i><span lang="">, <b>2021</b>, <i>31</i>,<i></i> 1-7.</span> </span><a href="https://doi.org/10.1016/j.mencom.2021.01.001" style="background-color: white; color: #00669b; font-family: arial; font-size: 14.85px; text-decoration-line: none;" target="_blank">Link</a> </p>Dmitryhttp://www.blogger.com/profile/06591522667018423627noreply@blogger.comtag:blogger.com,1999:blog-7310545556512779422.post-89077021417459044532021-07-13T03:52:00.000+03:002021-07-13T03:52:34.851+03:00<p> </p><div class="separator" style="clear: both; text-align: center;"><a href="https://1.bp.blogspot.com/-vIhHPb59TXA/YOzicU0VoSI/AAAAAAAAFc8/B3Zsc0Xaiu0TNPt_q3iqH8bhNvFLtvJ0ACNcBGAsYHQ/s800/86.gif" style="margin-left: 1em; margin-right: 1em;"><img border="0" data-original-height="560" data-original-width="800" height="448" src="https://1.bp.blogspot.com/-vIhHPb59TXA/YOzicU0VoSI/AAAAAAAAFc8/B3Zsc0Xaiu0TNPt_q3iqH8bhNvFLtvJ0ACNcBGAsYHQ/w640-h448/86.gif" width="640" /></a></div><b style="color: #494949; font-family: arial; font-size: 14.85px;">Patterning of various materials by the photochemical reaction of [(C5H5)Fe(C6H6)]+ complex with salicylate dyes</b><p></p><p></p><p style="background-color: white; color: #494949; font-family: arial, tahoma, helvetica, freesans, sans-serif; font-size: 14.85px;"><span style="font-family: arial;"><span lang="">A</span>. <span lang="">M</span>. Shved<span lang=""> - synthesis, tests<br />P. A. Zhmurov - synthesis, tests<br /></span><span lang="">E</span>. <span lang="">I</span>. <span lang="">Gutsul - UV-vis spectroscopy<br /></span><span lang=""><span face=""><span lang=""><span face="">D. S. Perekalin - idea, tests, head of the lab<br /><span face=""><span lang=""><i><span lang=""><br /></span></i></span></span></span></span></span></span></span></p><p style="background-color: white; color: #494949; font-family: arial, tahoma, helvetica, freesans, sans-serif; font-size: 14.85px;"><span style="font-family: arial;"><span lang=""><span face=""><span lang=""><span face=""><span face=""><i><span lang="">New. J. Chem.</span></i><span lang="">, <b>2020</b>, <i>44</i>,<i></i> 18157-18161.</span> </span><a href="https://doi.org/10.1039/D0NJ04221H" style="color: #00669b; text-decoration-line: none;" target="_blank">Link</a></span></span></span></span></span></p>Dmitryhttp://www.blogger.com/profile/06591522667018423627noreply@blogger.comtag:blogger.com,1999:blog-7310545556512779422.post-16272591485826135272020-08-30T13:01:00.003+03:002020-10-08T15:40:08.979+03:00<p></p><div class="separator" style="clear: both; text-align: center;"><a href="https://1.bp.blogspot.com/-Ff096ipwfS0/X0t4Ywvcc8I/AAAAAAAAExQ/_5jbzztqS-8Cf_wLwSnEQhjgFw0tvd5sQCNcBGAsYHQ/s356/85.gif" style="margin-left: 1em; margin-right: 1em;"><img border="0" data-original-height="317" data-original-width="356" src="https://1.bp.blogspot.com/-Ff096ipwfS0/X0t4Ywvcc8I/AAAAAAAAExQ/_5jbzztqS-8Cf_wLwSnEQhjgFw0tvd5sQCNcBGAsYHQ/s0/85.gif" /></a></div><b style="color: #494949; font-family: arial; font-size: 14.85px;"><div><b style="color: #494949; font-family: arial; font-size: 14.85px;"><br /></b></div>Rhodium catalysts with a chiral cyclopentadienyl ligand derived from natural R-myrtenal</b><p></p><p style="background-color: white; color: #494949; font-family: arial, tahoma, helvetica, freesans, sans-serif; font-size: 14.85px;"><span style="font-family: arial;"><span lang="">R</span>. <span lang="">A</span>. Pototskiy<span lang=""> - synthesis<br />A. M. Kolos - synthesis of complexes, catalysis<br /></span><span lang="">Y</span>. <span lang="">Y</span>. <span lang="">Nelyubina - X-ray<br /></span><span lang=""><span face=""><span lang=""><span face="">D. S. Perekalin - head of the lab<br /><span face=""><span lang=""><i><span lang=""><br /></span></i></span></span></span></span></span></span></span></p><p style="background-color: white; color: #494949; font-family: arial, tahoma, helvetica, freesans, sans-serif; font-size: 14.85px;"><span style="font-family: arial;"><span lang=""><span face=""><span lang=""><span face=""><span face=""><i><span lang="">Eur. J. Org. Chem.</span></i><span lang="">, <b>2020</b>, <i></i> 6019-6025.</span> </span><a href="https://chemistry-europe.onlinelibrary.wiley.com/doi/full/10.1002/ejoc.202001029" style="color: #00669b; text-decoration-line: none;" target="_blank">Link</a></span></span></span></span></span></p>Dmitryhttp://www.blogger.com/profile/06591522667018423627noreply@blogger.comtag:blogger.com,1999:blog-7310545556512779422.post-88372386855878559702020-08-30T12:57:00.004+03:002020-08-30T12:58:19.984+03:00<p></p><div class="separator" style="clear: both; text-align: center;"><a href="https://1.bp.blogspot.com/-BA6f9RMNHW4/X0t4AVt9t9I/AAAAAAAAExI/Ic7q7Pku3iQX8E6Dq6CgdQRjsTot8RN9gCNcBGAsYHQ/s502/83.gif" style="margin-left: 1em; margin-right: 1em;"><img border="0" data-original-height="202" data-original-width="502" src="https://1.bp.blogspot.com/-BA6f9RMNHW4/X0t4AVt9t9I/AAAAAAAAExI/Ic7q7Pku3iQX8E6Dq6CgdQRjsTot8RN9gCNcBGAsYHQ/s0/83.gif" /></a></div><p style="background-color: white; color: #494949; font-family: arial, tahoma, helvetica, freesans, sans-serif; font-size: 14.85px;"><b style="font-family: arial;">Unexpected antifungal activity of half-sandwich complexes with metal−iodine bonds</b></p><p><span style="color: #444444; font-family: arial;"><span><span lang="">N. N. Efimov</span></span><span style="background-color: white;"> - synthesis</span><span style="background-color: white;"><br /></span>D. A.
Loginov - synthesis, head of the group<br />M. Yu. Sharipov - antifungal activity<br />A. A. Nazarov - cytotoxicity studies<br /><span lang="" style="background-color: white;">Y</span><span style="background-color: white;">. </span><span lang="" style="background-color: white;">Y</span><span style="background-color: white;">. </span><span lang="" style="background-color: white;">Nelyubina - X-ray<br /></span><span style="background-color: white;">D. S. Perekalin - head of t</span><span style="background-color: white;">he lab</span></span></p><p><span style="font-family: arial;"><span face="" lang="" style="background-color: white; color: #494949; font-size: 14.85px;"><span face=""><span lang=""><span face=""><span face=""><span lang=""><i><span lang=""><br /></span></i></span></span></span></span></span></span></span></p><p style="background-color: white; color: #494949; font-family: arial, tahoma, helvetica, freesans, sans-serif; font-size: 14.85px;"><span style="font-family: arial;"><span lang=""><span face=""><span lang=""><span face=""><span face=""><i><span lang="">J. Organomet. Chem.</span></i><span lang="">, <b>2020</b>, <i>916</i>, 121272.</span> </span><a href="http://dx.doi.org/10.1016/j.jorganchem.2020.121272" style="color: #00669b; text-decoration-line: none;" target="_blank">Link</a></span></span></span></span></span></p>Dmitryhttp://www.blogger.com/profile/06591522667018423627noreply@blogger.comtag:blogger.com,1999:blog-7310545556512779422.post-35411279764541392222020-08-30T12:52:00.003+03:002020-08-30T12:58:31.622+03:00<p> </p><div class="separator" style="clear: both; text-align: center;"><a href="https://1.bp.blogspot.com/-jqyzRXQWOf4/X0t22dHupjI/AAAAAAAAEw8/NMXAHo3KeiUaF_gbmdQ9NH9AJikt20XJwCNcBGAsYHQ/s600/80.gif" style="margin-left: 1em; margin-right: 1em;"><img border="0" data-original-height="232" data-original-width="600" src="https://1.bp.blogspot.com/-jqyzRXQWOf4/X0t22dHupjI/AAAAAAAAEw8/NMXAHo3KeiUaF_gbmdQ9NH9AJikt20XJwCNcBGAsYHQ/s0/80.gif" /></a></div><p style="background-color: white; color: #494949; font-family: arial, tahoma, helvetica, freesans, sans-serif; font-size: 14.85px;"><b style="font-family: arial;">Synthesis of cyclopentadienyl iron complexes with substituted phenylene ligands via Suzuki coupling</b></p><p style="background-color: white; color: #494949; font-family: arial, tahoma, helvetica, freesans, sans-serif; font-size: 14.85px;"><span style="font-family: arial;"><span lang="">A</span>. <span lang="">M</span>. <span lang="">Shved - synthesis<br /></span><span lang="">Y</span>. <span lang="">Y</span>. <span lang="">Nelyubina - X-ray<br /></span><span lang=""><span face=""><span lang=""><span face="">D. S. Perekalin - head of the lab<br /><span face=""><span lang=""><i><span lang=""><br /></span></i></span></span></span></span></span></span></span></p><p style="background-color: white; color: #494949; font-family: arial, tahoma, helvetica, freesans, sans-serif; font-size: 14.85px;"><span style="font-family: arial;"><span lang=""><span face=""><span lang=""><span face=""><span face=""><i><span lang="">J. Organomet. Chem.</span></i><span lang="">, <b>2020</b>, <i>906</i>, 121061.</span> </span><a href="http://dx.doi.org/10.1016/j.jorganchem.2019.121061" style="color: #00669b; text-decoration-line: none;" target="_blank">Link</a></span></span></span></span></span></p>Dmitryhttp://www.blogger.com/profile/06591522667018423627noreply@blogger.comtag:blogger.com,1999:blog-7310545556512779422.post-60938435328860958512020-08-10T02:19:00.005+03:002020-08-10T02:27:17.240+03:00<div class="separator"><div class="separator" style="margin-left: 1em; margin-right: 1em; text-align: center;"><img border="0" data-original-height="153" data-original-width="538" src="https://1.bp.blogspot.com/-Fftiipx41AQ/XzCEY0CExfI/AAAAAAAAErw/v1VrGB0bobEsRMUQbqpvXwYHS_fTvgUDACNcBGAsYHQ/s0/84.gif" /></div></div><p><b style="font-family: arial;">Synthesis and reactivity
of the cyclobutadiene nickel bromide</b></p><p><span style="font-family: arial;"><span lang="">N. V. Shvydkiy - synthesis<br />E. A.
Dlin - synthesis<br />K. V. Ivanov - synthesis<br />A. G. Buyanovskaya - analytical methods<br /></span><span lang="">Y. V. Nelyubina - X-ray</span><br /><span lang=""><span face=""><span lang=""><span face="">D. S. Perekalin - head of the lab<br /><span face=""><span lang=""><i><span lang=""><br /></span></i></span></span></span></span></span></span></span></p><p><span style="font-family: arial;"><span lang=""><span face=""><span lang=""><span face=""><span face=""><i><span lang="">Dalton Trans.</span></i><span lang=""> <b>2020</b>, <i>49</i></span>, 6801−6806. </span><a href="http://dx.doi.org/10.1039/D0DT01510E" target="_blank">Link</a></span></span></span></span></span></p>Dmitryhttp://www.blogger.com/profile/06591522667018423627noreply@blogger.comtag:blogger.com,1999:blog-7310545556512779422.post-83403018679395554532020-08-10T02:15:00.003+03:002020-08-10T02:16:08.853+03:00<div class="separator" style="clear: both; text-align: center;"><div class="separator" style="margin-left: 1em; margin-right: 1em;"><img border="0" data-original-height="291" data-original-width="600" src="https://1.bp.blogspot.com/-12s0bzyROHo/XzCCwPyx8qI/AAAAAAAAErk/Fw3WU_n8RmM7gKU3vie4scodzluiZ2O0ACNcBGAsYHQ/s0/82.gif" /></div></div><p><b style="font-family: arial;">Variability of
Rh(III)-catalyzed reactions of aromatic oximes with alkenes</b></p><p><span style="font-family: arial;"><span lang="">E</span>. <span lang="">A</span>. <span lang="">Trifonova - synthesis<br /></span><span lang="">A</span>. <span lang="">A</span>. <span lang="">Komarova - synthesis<br /></span><span lang="">D</span>. <span lang="">Chusov - ideas, chiral chromatography</span><br /><span lang=""><span face=""><span lang=""><span face="">D. S. Perekalin - head of the lab<br /><span face=""><span lang=""><i><span lang=""><br /></span></i></span></span></span></span></span></span></span></p><p><span style="font-family: arial;"><span lang=""><span face=""><span lang=""><span face=""><span face=""><i><span lang="">Synlett</span></i><span lang="">, <b>2020</b>, <i>31</i>, 1117−1120.</span> </span><a href="http://dx.doi.org/10.1055/s-0040-1707961" target="_blank">Link</a></span></span></span></span></span></p>Dmitryhttp://www.blogger.com/profile/06591522667018423627noreply@blogger.comtag:blogger.com,1999:blog-7310545556512779422.post-21237334745856676412020-08-10T02:07:00.004+03:002020-08-11T19:40:45.514+03:00<div class="separator" style="clear: both; text-align: center;"><div class="separator" style="margin-left: 1em; margin-right: 1em;"><img border="0" data-original-height="141" data-original-width="382" src="https://1.bp.blogspot.com/-6q5-mjMRkYA/XzCBe7ZeixI/AAAAAAAAErY/HpYqx0MFwdUzE6bEYDh57PUyayjtlsXkQCNcBGAsYHQ/s0/81.gif" /></div></div><p><b style="font-family: arial; font-size: 12pt;">Reactions of arene
replacement in transition metal complexes</b></p><p><span style="font-family: arial;"><span lang="">N. V. </span><span lang="">Shvydkiy</span> - review<br /><span lang=""><span face=""><span lang=""><span face="">D. S. Perekalin - review, head of the lab<br />special thanks to E. E. Karslyan and N. L. Loskutova for initial work</span></span></span></span></span></p><p><span lang="" style="font-size: 12pt;"><span face=""><span lang="" style="font-family: arial; font-size: 12pt;"><span face=""><span lang="" style="font-size: 12pt;"><i><span lang="" style="font-size: 12pt;">Coord</span><span style="font-size: 12pt;">. </span><span lang="" style="font-size: 12pt;">Chem</span><span style="font-size: 12pt;">. </span><span lang="" style="font-size: 12pt;">Rev.</span></i><span lang="" style="font-size: 12pt;"> <b>2020</b>, <i>411</i>, 213238</span>.</span> </span><a href="http://dx.doi.org/10.1016/j.ccr.2020.213238" target="_blank">Link</a></span></span></span></p>Dmitryhttp://www.blogger.com/profile/06591522667018423627noreply@blogger.comtag:blogger.com,1999:blog-7310545556512779422.post-30633237781505909002020-08-10T02:04:00.003+03:002020-08-10T02:16:35.760+03:00<div class="separator" style="clear: both; text-align: center;"><div class="separator" style="margin-left: 1em; margin-right: 1em;"><img border="0" data-original-height="169" data-original-width="542" src="https://1.bp.blogspot.com/-aUyZQWRQHJ8/XzCAp8hPWLI/AAAAAAAAErM/-n7kcI5vQj8u_rsxj3Nh2-7dOVDHcu5qgCNcBGAsYHQ/s0/79.gif" /></div></div><p><b style="font-family: arial; font-size: 12pt;">Synthesis and reactivity
of heptamethylcyclohexadienyl rhodium(III) complexes</b></p><p><span style="font-family: arial;"><span lang="">R. A. </span><span lang="">Pototskiy</span> - synthesis<br /><span lang=""><span face=""><span lang=""><span face="">Y. V. Nelyubina - X-ray<br />D. S. Perekalin - head of the lab</span></span></span></span></span></p><p><span lang="" style="font-size: 12pt;"><span face=""><span lang="" style="font-family: arial; font-size: 12pt;"><span face=""><i><span lang="" style="font-size: 12pt;">Organometallics</span></i><span lang="" style="font-size: 12pt;"> <b>2019</b>, 38, 4607–4614.</span> </span><a href="http://dx.doi.org/10.1021/acs.organomet.9b00621" target="_blank">Link</a></span></span></span></p>Dmitryhttp://www.blogger.com/profile/06591522667018423627noreply@blogger.com