MULTIPLE BONDS BETWEEN TRANSITION-METALS AND MAIN-GROUP ELEMENTS .142. LEWIS-BASE ADDUCTS OF ORGANORHENIUM(VII) OXIDES - STRUCTURES AND DYNAMIC BEHAVIOR IN SOLUTION

被引:72
作者
HERRMANN, WA
KUHN, FE
RAUCH, MU
CORREIA, JDG
ARTUS, G
机构
[1] Anorganisch-chemisches Institut, Technischen Universität München, D-85747 Garching b. München
关键词
D O I
10.1021/ic00115a019
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Organorhenium(VII) oxides such as methyltrioxorhenium(VII) (1) and its longer-chain alkyl derivatives form 1:1 and 1:2 adducts with nitrogen-donor Lewis bases. These compounds adopt well-defined structures in the solid state. In solution, they undergo exchange of both the metal-coordinated base ligands and the oxo ligands. The synthesis and crystal structure (X-ray diffraction study) of the amino-functionalized complex O3Re-CH2CH2CH2N(C5H10) (3a) is reported. Crystal data are as follows: monoclinic, space group P2(1)/c, a = 8.327(2) Angstrom, b = 11.516(1) Angstrom, c = 10.864(2) Angstrom, beta = 101.54(7)degrees R = 0.028 for 1747 reflections. Compounds of type 3a are intramolecular base adducts in the solid state, but rigid geometries in solution can only be observed at low temperatures.
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页码:2914 / 2920
页数:7
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