Synthesis, structure, and chemistry of new, mixed group 14 and 16 heterocycles: Nucleophile-induced ring contraction of mesocyclic dications

被引:38
作者
Block, Eric [1 ]
Dikarev, Evgeny V.
Glass, Richard S.
Jin, Jin
Li, Bo
Li, Xiaojie
Zhang, Shao-Zhong
机构
[1] SUNY Albany, Dept Chem, Albany, NY 12222 USA
[2] Univ Arizona, Tucson, AZ 85721 USA
关键词
D O I
10.1021/ja065037j
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
More than 40 new 4- to 12-membered ring heterocycles containing various combinations of Group 14 and 16 elements Si, Sn, S, Se, and Te have been synthesized and fully characterized. Synthesis of these small-ring as well as medium-ring ( mesocyclic) heterocycles from alpha, omega-dihalides is facilitated by the presence of gem-dialkylsilyl and gem-dialkylstannyl groups in the precursors. Conformations of several of the new ring systems in the solid state have been determined by X-ray crystal structure analysis. Oxidation of mixed S( Se, Te)/Si eight-membered ring mesocycles with NOPF6 or Br-2 gives dications or a bicyclic dibromide, respectively, which can be characterized by NMR methods. On treatment with nucleophiles, mesocyclic dications, or the corresponding radical cations undergo ring contraction, giving five- or six-membered ring heterocycles. Photolysis of a S/Se four-membered ring heterocycle gives selenoformaldehyde, trapped in 80% yield with 2,3-dimethyl-1,3-butadiene.
引用
收藏
页码:14949 / 14961
页数:13
相关论文
共 117 条
[1]   A new route to polyselenoether macrocycles. Catalytic macrocyclization of 3,3-dimethylselenetane by Re-2(CO)(9)SeCH2CMe2CH2 [J].
Adams, RD ;
McBride, KT ;
Rogers, RD .
ORGANOMETALLICS, 1997, 16 (18) :3895-3901
[2]   NEW CYCLIC TELLURIDES - SYNTHESIS, REACTION AND LIGAND PROPERTIES OF 2,2,6,6-TETRAMETHYL-1-OXA-4-TELLURA-2,6-DISILACYCLOHEXANE (C6H16OSI2TE) - X-RAY STRUCTURE DETERMINATION OF C6H16OSI2TEI2 [J].
ALRUBAIE, AZ ;
UEMURA, S ;
MASUDA, H .
JOURNAL OF ORGANOMETALLIC CHEMISTRY, 1991, 410 (03) :309-320
[3]   FORMATION OF THE TRANSIENT TELLUROKETONE (1R)-3-TELLUROXOCAMPHOR AND ITS DIMERIZATION TO THE CORRESPONDING SYN-1,3-DITELLURETANES AND ANTI-1,3-DITELLURETANES [J].
BACK, TG ;
DYCK, BP ;
PARVEZ, M .
JOURNAL OF ORGANIC CHEMISTRY, 1995, 60 (14) :4657-4659
[4]   3,3-DIALKYL 3-GERMA THIETANES - SYNTHESIS AND REACTIVITY [J].
BARRAU, J ;
RIMA, G ;
SATGE, J .
SYNTHESIS AND REACTIVITY IN INORGANIC AND METAL-ORGANIC CHEMISTRY, 1984, 14 (01) :21-37
[5]   DIALKYL-3,3 GERMA-3 THIETANNES [J].
BARRAU, J ;
RIMA, G ;
SATGE, J .
JOURNAL OF ORGANOMETALLIC CHEMISTRY, 1983, 252 (03) :C73-C77
[6]   THERMOLYSIS, PYROLYSIS AND PHOTOLYSIS OF GERMYLATED AND SULFATED HETEROCYCLES WITH 4 AND 5 GROUPS - INTERMEDIATE SPECIES WITH DOUBLY-BONDED GERMANIUM [J].
BARRAU, J ;
RIMA, G ;
ELAMINE, M ;
SATGE, J .
JOURNAL OF ORGANOMETALLIC CHEMISTRY, 1988, 345 (1-2) :39-50
[7]  
BASSINDALE AR, 1989, CHEM ORGANIC SILICON, V2, P893
[8]   Synthesis, characterization, and redox behavior of new selenium coronands and of copper(I) and copper(II) complexes of selenium coronands [J].
Batchelor, RJ ;
Einstein, FWB ;
Gay, ID ;
Gu, JH ;
Mehta, S ;
Pinto, BM ;
Zhou, XM .
INORGANIC CHEMISTRY, 2000, 39 (12) :2558-2571
[9]   Tetrahydrofuran analogues with silicon and sulphur atoms [J].
Berthier, G ;
Cadioli, B ;
Gallinella, E .
THEORETICAL CHEMISTRY ACCOUNTS, 2000, 104 (3-4) :223-225
[10]   CHEMISTRY OF THIOETHER MACROCYCLIC COMPLEXES [J].
Blake, Alexander J. ;
Schroeder, Martin .
ADVANCES IN INORGANIC CHEMISTRY <D>, 1990, 35 :1-80