C-S BOND-CLEAVAGE AT AN ELECTROPHILIC ZIRCONIUM CENTER - SYNTHESIS, STRUCTURE, AND THERMAL-DECOMPOSITION OF [CP2ZR(S-TERT-C4H9)(THF)][BPH4]

被引：31

作者：

PIERS, WE ^{[1
]}

KOCH, L ^{[1
]}

RIDGE, DS ^{[1
]}

MACGILLIVRAY, LR ^{[1
]}

ZAWOROTKO, M ^{[1
]}

机构：

[1] ST MARYS UNIV, DEPT CHEM, HALIFAX B3H 3C3, NS, CANADA

来源：

ORGANOMETALLICS | 1992年 / 11卷 / 09期

关键词：

D O I：

10.1021/om00045a036

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

Protonolysis of [Cp2ZrCH3(THF)] [BPh4] With tert-butyl mercaptan leads to the (thiolato)zirconocene Cation [Cp2Zr(S-t-C4H9)(THF)] [BPh4] in 79 % yield. In addition to the usual spectroscopic methods the complex was characterized by X-ray crystallography (monoclinic, P2(1)/c, a = 10.111 (4) angstrom, b = 18.6066 (18) angstrom, c = 19.408 (7) angstrom, beta = 94.31 (2)-degrees, Z = 4, R = 0.036). Structural Parameters and THF exchange rates point to a less electrophilic Zr center than in the parent alkyl species. Nevertheless, the center is electrophilic enough to induce C-S bond cleavage under thermal duress.

引用

页码：3148 / 3152

页数：5

共 30 条

[21] STRUCTURE AND CHEMISTRY OF BIS(CYCLOPENTADIENYL)-MLN COMPLEXES [J].