Group 14 and 15 heteroallenes E=C=C and E=C=E′

被引:78
作者
Escudie, Jean [1 ]
Ranaivonjatovo, Henri [1 ]
机构
[1] Univ Toulouse 3, UMR 5069, F-31062 Toulouse 09, France
关键词
D O I
10.1021/om0610086
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
This review describes the synthesis, physical properties, and some aspects of the reactivity of heteroallenes, namely the heavier congeners of allenes containing one or two doubly bonded heavier elements of groups 14 (Si, Ge, Sn) and 15 (P, As, Sb). The key factor for their preparation lies in the use of synthetic methods effective under mild conditions: i.e., in many cases, the dehalogenation at low temperature of dihaloheteropropenes by lithium derivatives. Their stabilization was successful, owing to very bulky substituents; substituted aromatic groups were often used, particularly the 2,4,6-tri-tert-butylphenyl group (supermesityl). Whereas various types of heteroallenes containing a doubly bonded element of the second or third long row have been isolated, their heavier counterparts of the fourth row have only been postulated as reaction intermediates.
引用
收藏
页码:1542 / 1559
页数:18
相关论文
共 193 条
[1]   Synthesis, structure, and bonding of stable dialkylsilaketenimines [J].
Abe, T ;
Iwamoto, T ;
Kabuto, C ;
Kira, M .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2006, 128 (13) :4228-4229
[2]   DIFFERENT MODES OF HYDROGEN MIGRATION IN REACTIONS OF DIPHOSPHAALLENE, ARP=C=PAR (AR = 2,4,6-BU(T)3C6H2) WITH [W(CO)5(THF)] AND [FE3(CO)12].CRYSTAL AND MOLECULAR-STRUCTURE OF [FE2(CO)6(ARP=CHPCH2(CME2)C6H2BU(T)2] [J].
AKPAN, CA ;
HITCHCOCK, PB ;
NIXON, JF ;
YOSHIFUJI, M ;
NIITSU, T ;
INAMOTO, N .
JOURNAL OF ORGANOMETALLIC CHEMISTRY, 1988, 338 (03) :C35-C37
[3]   EPR characterization of new phosphavinyl sigma radicals [J].
Alberti, A ;
Benaglia, M ;
DellaBona, MA ;
Guerra, M ;
Hudson, A ;
Macciantelli, D .
RESEARCH ON CHEMICAL INTERMEDIATES, 1996, 22 (04) :381-392
[4]   A gem-aluminium(III)/antimony(III) C centre incorporated in a bimetallic six-membered heterocycle [J].
Andrews, PC ;
Raston, CL ;
Skelton, BW ;
White, AH .
CHEMICAL COMMUNICATIONS, 1997, (13) :1183-1184
[5]   Carbometalation of a stiba-alkene resulting in an In(III)/Sb(III) C-centered geminal organodimetallic complex [J].
Andrews, PC ;
Nichols, PJ ;
Raston, CL ;
Roberts, BA .
ORGANOMETALLICS, 1999, 18 (21) :4247-4249
[6]   Decomposition of [2-Pyr(SiMe3)2C]2SbCl into the stibaalkene [2-Pyr(SiMe3)2C-Sb=C(SiMe3)2-Pyr]:: Solid, solution, and a initio study [J].
Andrews, PC ;
McGrady, JE ;
Nichols, PJ .
ORGANOMETALLICS, 2004, 23 (03) :446-453
[7]   Gallium(III)/antimony(III) C-centered geminal organodimetallic complexes [J].
Andrews, PC ;
Nichols, PJ .
ORGANOMETALLICS, 2000, 19 (07) :1277-1281
[8]  
[Anonymous], 1991, HETEROATOM CHEM
[9]   A COMPOUND WITH A TIN-CARBON DOUBLE-BOND, BIS(2,4,6-TRIISOPROPYLPHENYL)(FLUORENYLIDENE)STANNANE - ASPECTS OF ITS REACTIVITY AND X-RAY STRUCTURE OF ITS DIMER [J].
ANSELME, G ;
DECLERCQ, JP ;
DUBOURG, A ;
RANAIVONJATOVO, H ;
ESCUDIE, J ;
COURET, C .
JOURNAL OF ORGANOMETALLIC CHEMISTRY, 1993, 458 (1-2) :49-56
[10]   A STABLE COMPOUND WITH A FORMAL TIN CARBON DOUBLE-BOND - THE BIS(2,4,6-TRIISOPROPYLPHENYL)(FLUORENYLIDENE)STANNENE [J].
ANSELME, G ;
RANAIVONJATOVO, H ;
ESCUDIE, J ;
COURET, C ;
SATGE, J .
ORGANOMETALLICS, 1992, 11 (08) :2748-2750