Metallaaromatic biaryl atropisomers
Synthesis of stable irida-binaphthyl and -phenanthryl complexes, the first examples of metallaaromatic biaryl atropisomers, has been achieved. The combination of experimental and theoretical studies revealed that the nature of these systems is comparable to that of well-known 1,1′-binaphthalene both...
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Veröffentlicht in: | Chemical communications (Cambridge, England) England), 2018-09, Vol.54 (78), p.1974-1976 |
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container_end_page | 1976 |
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container_issue | 78 |
container_start_page | 1974 |
container_title | Chemical communications (Cambridge, England) |
container_volume | 54 |
creator | Talavera, M Peña-Gallego, A Alonso-Gómez, J. L Bolaño, S |
description | Synthesis of stable irida-binaphthyl and -phenanthryl complexes, the first examples of metallaaromatic biaryl atropisomers, has been achieved. The combination of experimental and theoretical studies revealed that the nature of these systems is comparable to that of well-known 1,1′-binaphthalene both in terms of aromaticity and atropisomerism.
The birth of metallaaromatic biaryl atropisomers: synthesis, structural elucidation, and theoretical analysis of the first examples is reported. |
doi_str_mv | 10.1039/c8cc06443a |
format | Article |
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The birth of metallaaromatic biaryl atropisomers: synthesis, structural elucidation, and theoretical analysis of the first examples is reported.</description><subject>Aromaticity</subject><subject>Mass spectra</subject><subject>NMR</subject><subject>Nuclear magnetic resonance</subject><issn>1359-7345</issn><issn>1364-548X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNpdkE1LAzEQhoMotlYv3hWhFxFWJ5uvzbEsfkHFi4K3JTtNYMtuU5Pdg__e1NYK5jJh5mGY9yHknMItBabvsEAEyTkzB2RMmeSZ4MXH4eYvdKYYFyNyEuMS0qOiOCYjBjlozosxmb7Y3rStMcF3pm_wqm5M-GqvTB_8uom-syGekiNn2mjPdnVC3h_u38qnbP76-FzO5hkypvrMGiM15Uqj4tqAEk4aJmvnrOROU-RAa4WuFlDnDgCRoxGQu9RZAKWCTcj1du86-M_Bxr7qmog2XbeyfohVntJKJbiAhE7_oUs_hFW6LlE0lylp8jEhN1sKg48xWFetQ9OlfBWFaqOuKouy_FE3S_DlbuVQd3axR39dJeBiC4SI--mfe_YNR9dxMw</recordid><startdate>20180927</startdate><enddate>20180927</enddate><creator>Talavera, M</creator><creator>Peña-Gallego, A</creator><creator>Alonso-Gómez, J. L</creator><creator>Bolaño, S</creator><general>Royal Society of Chemistry</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-2635-4133</orcidid><orcidid>https://orcid.org/0000-0002-5013-9831</orcidid><orcidid>https://orcid.org/0000-0002-6107-0120</orcidid><orcidid>https://orcid.org/0000-0002-6898-8305</orcidid></search><sort><creationdate>20180927</creationdate><title>Metallaaromatic biaryl atropisomers</title><author>Talavera, M ; Peña-Gallego, A ; Alonso-Gómez, J. L ; Bolaño, S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c337t-eaa691479c749a075f6a36bffe64f91c401b7cfb50b2f00cc4ca502ffb5d01153</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Aromaticity</topic><topic>Mass spectra</topic><topic>NMR</topic><topic>Nuclear magnetic resonance</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Talavera, M</creatorcontrib><creatorcontrib>Peña-Gallego, A</creatorcontrib><creatorcontrib>Alonso-Gómez, J. L</creatorcontrib><creatorcontrib>Bolaño, S</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>MEDLINE - Academic</collection><jtitle>Chemical communications (Cambridge, England)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Talavera, M</au><au>Peña-Gallego, A</au><au>Alonso-Gómez, J. L</au><au>Bolaño, S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Metallaaromatic biaryl atropisomers</atitle><jtitle>Chemical communications (Cambridge, England)</jtitle><addtitle>Chem Commun (Camb)</addtitle><date>2018-09-27</date><risdate>2018</risdate><volume>54</volume><issue>78</issue><spage>1974</spage><epage>1976</epage><pages>1974-1976</pages><issn>1359-7345</issn><eissn>1364-548X</eissn><abstract>Synthesis of stable irida-binaphthyl and -phenanthryl complexes, the first examples of metallaaromatic biaryl atropisomers, has been achieved. The combination of experimental and theoretical studies revealed that the nature of these systems is comparable to that of well-known 1,1′-binaphthalene both in terms of aromaticity and atropisomerism.
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source | Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection |
subjects | Aromaticity Mass spectra NMR Nuclear magnetic resonance |
title | Metallaaromatic biaryl atropisomers |
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