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Synthesis, Substitution, and Oxidation of Imidazole‐2‐thione Based Tricyclic 1,4‐Dihydro‐1,4‐diphosphinines
Herein, the synthesis and chemistry of P‐functional tricyclic 1,4‐dihydro‐1,4‐diphosphinines is described, following a recent communication on their use as precursors of 1,4‐diphosphinines. In particular, ring formation of imidazole‐2‐thione‐based tricyclic 1,4‐dihydro‐1,4‐diphosphinines 4a,b {–[P(M...
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Published in: | European journal of inorganic chemistry 2018-02, Vol.2018 (7), p.904-916 |
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description | Herein, the synthesis and chemistry of P‐functional tricyclic 1,4‐dihydro‐1,4‐diphosphinines is described, following a recent communication on their use as precursors of 1,4‐diphosphinines. In particular, ring formation of imidazole‐2‐thione‐based tricyclic 1,4‐dihydro‐1,4‐diphosphinines 4a,b {–[P(Me2N)IMSR,R]2–; IMSR,R = 1,3‐dialkylimidazole‐2‐thione‐4‐yl}, first detected as side products, has been optimized to access 4d–f {–[P(Et2N)IMSR,R]2–; IMSR,R = 1,3‐dialkylimidazole‐2‐thione‐4‐yl}. The 1,4‐dihydro‐1,4‐dichloro‐1,4‐diphosphinines 8a,b {–[P(Cl)IMSR,R]2–; IMSR,R = 1,3‐dialkylimidazole‐2‐thione‐4‐yl}, easily obtained from 4, are ideal starting materials for P‐substituted products 9a–c (P–R; R = nBu, TMSC2–). The P‐diorganoamino derivatives 4d–f are used to synthesize bis(P–oxides) 10a–c and bis(P‐sulfides) 11a–c, and similarly, the bis(P–borane) adducts 13a–c. The first examples of bis(spirophosphorane) derivatives 12a–c, featuring two benzodioxaphosphole units, are synthesized by the reaction of 4d–f with o‐chloranil. Attempts to access bis(phosphonium) derivatives using methyl trifluoromethanesulfonate have resulted in S‐methylation of 4d–f, and hence, have furnished the first examples of tricyclic 1,4‐dihydro‐1,4‐diphosphinines possessing two imidazolium units 14a,b {[–{P(Me2N)‐IMSMeR,R}2–](CF3SO3)2; IMSMeR,R = 1,3‐dialkyl‐2‐thiomethyl‐imidazolium‐4‐yl}.
Imidazole‐2‐thione‐based tricyclic 1,4‐dihydro‐1,4‐diphosphinines II were synthesized by LDA‐induced cyclization starting from moncyclic 1,4‐dihydro‐1,4‐diphosphinines ; the molecular electrostatic potential indicates competing nucleophilic centers. |
doi_str_mv | 10.1002/ejic.201701338 |
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Imidazole‐2‐thione‐based tricyclic 1,4‐dihydro‐1,4‐diphosphinines II were synthesized by LDA‐induced cyclization starting from moncyclic 1,4‐dihydro‐1,4‐diphosphinines ; the molecular electrostatic potential indicates competing nucleophilic centers.</description><identifier>ISSN: 1434-1948</identifier><identifier>EISSN: 1099-0682</identifier><identifier>DOI: 10.1002/ejic.201701338</identifier><language>eng</language><publisher>Weinheim: Wiley Subscription Services, Inc</publisher><subject>Adducts ; Chemical synthesis ; Derivatives ; Electrostatic interactions ; Imidazole ; Inorganic chemistry ; Methylation ; Oxidation ; Phosphorus heterocycles ; P–borane adduct ; S methylation ; Substituent effects ; Substitution reactions</subject><ispartof>European journal of inorganic chemistry, 2018-02, Vol.2018 (7), p.904-916</ispartof><rights>2018 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3178-2e3c3cdc79600dd83a9cb4a8a03c4107d559ac40adbaec357e93de6d8ff992a83</citedby><cites>FETCH-LOGICAL-c3178-2e3c3cdc79600dd83a9cb4a8a03c4107d559ac40adbaec357e93de6d8ff992a83</cites><orcidid>0000-0001-7840-2139 ; 0000-0001-5661-8502 ; 0000-0002-5793-781X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Koner, Abhishek</creatorcontrib><creatorcontrib>Sauerbrey, Susanne</creatorcontrib><creatorcontrib>Schnakenburg, Gregor</creatorcontrib><creatorcontrib>Bauzá, Antonio</creatorcontrib><creatorcontrib>Frontera, Antonio</creatorcontrib><creatorcontrib>Streubel, Rainer</creatorcontrib><title>Synthesis, Substitution, and Oxidation of Imidazole‐2‐thione Based Tricyclic 1,4‐Dihydro‐1,4‐diphosphinines</title><title>European journal of inorganic chemistry</title><description>Herein, the synthesis and chemistry of P‐functional tricyclic 1,4‐dihydro‐1,4‐diphosphinines is described, following a recent communication on their use as precursors of 1,4‐diphosphinines. In particular, ring formation of imidazole‐2‐thione‐based tricyclic 1,4‐dihydro‐1,4‐diphosphinines 4a,b {–[P(Me2N)IMSR,R]2–; IMSR,R = 1,3‐dialkylimidazole‐2‐thione‐4‐yl}, first detected as side products, has been optimized to access 4d–f {–[P(Et2N)IMSR,R]2–; IMSR,R = 1,3‐dialkylimidazole‐2‐thione‐4‐yl}. The 1,4‐dihydro‐1,4‐dichloro‐1,4‐diphosphinines 8a,b {–[P(Cl)IMSR,R]2–; IMSR,R = 1,3‐dialkylimidazole‐2‐thione‐4‐yl}, easily obtained from 4, are ideal starting materials for P‐substituted products 9a–c (P–R; R = nBu, TMSC2–). The P‐diorganoamino derivatives 4d–f are used to synthesize bis(P–oxides) 10a–c and bis(P‐sulfides) 11a–c, and similarly, the bis(P–borane) adducts 13a–c. The first examples of bis(spirophosphorane) derivatives 12a–c, featuring two benzodioxaphosphole units, are synthesized by the reaction of 4d–f with o‐chloranil. Attempts to access bis(phosphonium) derivatives using methyl trifluoromethanesulfonate have resulted in S‐methylation of 4d–f, and hence, have furnished the first examples of tricyclic 1,4‐dihydro‐1,4‐diphosphinines possessing two imidazolium units 14a,b {[–{P(Me2N)‐IMSMeR,R}2–](CF3SO3)2; IMSMeR,R = 1,3‐dialkyl‐2‐thiomethyl‐imidazolium‐4‐yl}.
Imidazole‐2‐thione‐based tricyclic 1,4‐dihydro‐1,4‐diphosphinines II were synthesized by LDA‐induced cyclization starting from moncyclic 1,4‐dihydro‐1,4‐diphosphinines ; the molecular electrostatic potential indicates competing nucleophilic centers.</description><subject>Adducts</subject><subject>Chemical synthesis</subject><subject>Derivatives</subject><subject>Electrostatic interactions</subject><subject>Imidazole</subject><subject>Inorganic chemistry</subject><subject>Methylation</subject><subject>Oxidation</subject><subject>Phosphorus heterocycles</subject><subject>P–borane adduct</subject><subject>S methylation</subject><subject>Substituent effects</subject><subject>Substitution reactions</subject><issn>1434-1948</issn><issn>1099-0682</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNqFULFOwzAUtBBIlMLKbIm1Kc-xm9gjlAJFlTq0zJFrO4qrNA5xIggTn8A38iUkCoKR4end6e7ekw6hSwJTAhBem71V0xBIDIRSfoRGBIQIIOLhcYcZZQERjJ-iM-_3AECBRiPUbNqizoy3foI3zc7Xtm5q64oJloXG6zerZU-xS_Hy0JF3l5uvj8-wmzrrBINvpTcabyurWpVbhcmEdeKdzVpduQ4NXNsyc77MbGEL48_RSSpzby5-9hg93y-288dgtX5Yzm9WgaIk5kFoqKJKq1hEAFpzKoXaMcklUMUIxHo2E1IxkHonjaKz2AiqTaR5mgoRSk7H6Gq4W1bupTG-TvauqYruZRICRDHjIuxd08GlKud9ZdKkrOxBVm1CIOmrTfpqk99qu4AYAq82N-0_7mTxtJz_Zb8B_kSDTg</recordid><startdate>20180221</startdate><enddate>20180221</enddate><creator>Koner, Abhishek</creator><creator>Sauerbrey, Susanne</creator><creator>Schnakenburg, Gregor</creator><creator>Bauzá, Antonio</creator><creator>Frontera, Antonio</creator><creator>Streubel, Rainer</creator><general>Wiley Subscription Services, Inc</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope><orcidid>https://orcid.org/0000-0001-7840-2139</orcidid><orcidid>https://orcid.org/0000-0001-5661-8502</orcidid><orcidid>https://orcid.org/0000-0002-5793-781X</orcidid></search><sort><creationdate>20180221</creationdate><title>Synthesis, Substitution, and Oxidation of Imidazole‐2‐thione Based Tricyclic 1,4‐Dihydro‐1,4‐diphosphinines</title><author>Koner, Abhishek ; Sauerbrey, Susanne ; Schnakenburg, Gregor ; Bauzá, Antonio ; Frontera, Antonio ; Streubel, Rainer</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3178-2e3c3cdc79600dd83a9cb4a8a03c4107d559ac40adbaec357e93de6d8ff992a83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Adducts</topic><topic>Chemical synthesis</topic><topic>Derivatives</topic><topic>Electrostatic interactions</topic><topic>Imidazole</topic><topic>Inorganic chemistry</topic><topic>Methylation</topic><topic>Oxidation</topic><topic>Phosphorus heterocycles</topic><topic>P–borane adduct</topic><topic>S methylation</topic><topic>Substituent effects</topic><topic>Substitution reactions</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Koner, Abhishek</creatorcontrib><creatorcontrib>Sauerbrey, Susanne</creatorcontrib><creatorcontrib>Schnakenburg, Gregor</creatorcontrib><creatorcontrib>Bauzá, Antonio</creatorcontrib><creatorcontrib>Frontera, Antonio</creatorcontrib><creatorcontrib>Streubel, Rainer</creatorcontrib><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><jtitle>European journal of inorganic chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Koner, Abhishek</au><au>Sauerbrey, Susanne</au><au>Schnakenburg, Gregor</au><au>Bauzá, Antonio</au><au>Frontera, Antonio</au><au>Streubel, Rainer</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis, Substitution, and Oxidation of Imidazole‐2‐thione Based Tricyclic 1,4‐Dihydro‐1,4‐diphosphinines</atitle><jtitle>European journal of inorganic chemistry</jtitle><date>2018-02-21</date><risdate>2018</risdate><volume>2018</volume><issue>7</issue><spage>904</spage><epage>916</epage><pages>904-916</pages><issn>1434-1948</issn><eissn>1099-0682</eissn><abstract>Herein, the synthesis and chemistry of P‐functional tricyclic 1,4‐dihydro‐1,4‐diphosphinines is described, following a recent communication on their use as precursors of 1,4‐diphosphinines. In particular, ring formation of imidazole‐2‐thione‐based tricyclic 1,4‐dihydro‐1,4‐diphosphinines 4a,b {–[P(Me2N)IMSR,R]2–; IMSR,R = 1,3‐dialkylimidazole‐2‐thione‐4‐yl}, first detected as side products, has been optimized to access 4d–f {–[P(Et2N)IMSR,R]2–; IMSR,R = 1,3‐dialkylimidazole‐2‐thione‐4‐yl}. The 1,4‐dihydro‐1,4‐dichloro‐1,4‐diphosphinines 8a,b {–[P(Cl)IMSR,R]2–; IMSR,R = 1,3‐dialkylimidazole‐2‐thione‐4‐yl}, easily obtained from 4, are ideal starting materials for P‐substituted products 9a–c (P–R; R = nBu, TMSC2–). The P‐diorganoamino derivatives 4d–f are used to synthesize bis(P–oxides) 10a–c and bis(P‐sulfides) 11a–c, and similarly, the bis(P–borane) adducts 13a–c. The first examples of bis(spirophosphorane) derivatives 12a–c, featuring two benzodioxaphosphole units, are synthesized by the reaction of 4d–f with o‐chloranil. Attempts to access bis(phosphonium) derivatives using methyl trifluoromethanesulfonate have resulted in S‐methylation of 4d–f, and hence, have furnished the first examples of tricyclic 1,4‐dihydro‐1,4‐diphosphinines possessing two imidazolium units 14a,b {[–{P(Me2N)‐IMSMeR,R}2–](CF3SO3)2; IMSMeR,R = 1,3‐dialkyl‐2‐thiomethyl‐imidazolium‐4‐yl}.
Imidazole‐2‐thione‐based tricyclic 1,4‐dihydro‐1,4‐diphosphinines II were synthesized by LDA‐induced cyclization starting from moncyclic 1,4‐dihydro‐1,4‐diphosphinines ; the molecular electrostatic potential indicates competing nucleophilic centers.</abstract><cop>Weinheim</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1002/ejic.201701338</doi><tpages>13</tpages><orcidid>https://orcid.org/0000-0001-7840-2139</orcidid><orcidid>https://orcid.org/0000-0001-5661-8502</orcidid><orcidid>https://orcid.org/0000-0002-5793-781X</orcidid></addata></record> |
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subjects | Adducts Chemical synthesis Derivatives Electrostatic interactions Imidazole Inorganic chemistry Methylation Oxidation Phosphorus heterocycles P–borane adduct S methylation Substituent effects Substitution reactions |
title | Synthesis, Substitution, and Oxidation of Imidazole‐2‐thione Based Tricyclic 1,4‐Dihydro‐1,4‐diphosphinines |
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