SYNTHESIS AND STRUCTURE OF NI(2,6-IPR2C6H3N=CH-CH=NC6H3-2,6-IPR2)2

被引：11

作者：

BONRATH, W ^{[1
]}

PORSCHKE, KR ^{[1
]}

MYNOTT, R ^{[1
]}

KRUGER, C ^{[1
]}

机构：

[1] MAX PLANCK INST COAL RES,POSTFACH 101353,W-4330 MULHEIM,GERMANY

来源：

ZEITSCHRIFT FUR NATURFORSCHUNG SECTION B-A JOURNAL OF CHEMICAL SCIENCES | 1990年 / 45卷 / 12期

关键词：

1,4-DIAZADIENE; NICKEL(0); X-RAY;

D O I：

10.1515/znb-1990-1209

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

Ni(cdt)** reacts with two equivalents of the sterically highly demanding 1,4-diazadiene 2,6-(i)Pr2C6H3N = CH-CH = NC6H3-2,6(i)Pr2 to yield the red-brown, crystalline title compound Ni(2,6-(i)Pr2Ph-dad)2 (3). The existence of this compound was previously uncertain. H-1 and C-13 NMR, MS, and UV/VIS spectra of 3 are reported. The X-ray structure analysis of 3 revealed a strongly distored tetrahedral coordination of the nickel center with a dihedral angle of 51-degrees between the planes of the chelate rings and mean bond lengths Ni-N 1.965(4) angstrom and N = CH 1.308(5) angstrom. The poorly soluble compound appears to be rather unreactive because of the bulk of the ligands.

引用

页码：1647 / 1650

页数：4

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