首页> 外文期刊>Journal of Organometallic Chemistry >SYNTHESIS, STRUCTURE AND PROPERTIES OF NEW TRANSITION METAL COMPLEXES OF 9,10-DIHYDRO-9,10-DIMETHYL-9,10-DIBORAANTHRACENE [German]
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SYNTHESIS, STRUCTURE AND PROPERTIES OF NEW TRANSITION METAL COMPLEXES OF 9,10-DIHYDRO-9,10-DIMETHYL-9,10-DIBORAANTHRACENE [German]

机译:9,10-二氢-9,10-二甲基-9,10-二硼烷蒽的新型过渡金属配合物的合成,结构和性质[德语]

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摘要

Reactions of 9,10-Dihydro-9,10-dimethyl-9,10-diboraanthracene (1) with the isolobal 14 VE metal complex fragments Ru(CO)(3), Co(C5H5), Fe(C7H8) and Ni(C8H12) yield the 18 VE compounds 2, 3, 4, and 5. With (CO)(3)Cr(CH3CN)(3) complexation takes place at the carbacyclic moiety of 1 to give 6. Neither reduction nor carbonylation of 6 at 40 bar CO pressure result in a slippage of the chromium carbonyl group towards the heterocyclic part of 1. The reaction of 3 with (CO)(3)Cr(CH3CN)(3) leads to the 34 VE ''slipped'' triple-decker 7. The complexes 2, 3, and 4 are reversibly reduced to give the paramagnetic 19 VE monoanions. The electrochemistry of 2, 3, and 4 as well as ESR data of 3(-) and 4(-) are reported. The constitutions of 2, 3, 4, and 5 have been confirmed by X-ray structure analyses. [References: 41]
机译:9,10-二氢-9,10-二甲基-9,10-二硼蒽蒽(1)与等规14 VE金属配合物片段Ru(CO)(3),Co(C5H5),Fe(C7H8)和Ni( C8H12)生成18个VE化合物2、3、4和5。通过(CO)(3)Cr(CH3CN)(3),在1的碳环部分发生络合,得到6。6处的还原或羰基化均不发生。 40 bar CO压力导致羰基铬羰基向1的杂环部分滑移。3与(CO)(3)Cr(CH3CN)(3)的反应导致34 VE“滑移”的三重双层7。将络合物2、3和4可逆地还原,得到顺磁性的19 VE单阴离子。报告了2、3和4的电化学以及3(-)和4(-)的ESR数据。通过X射线结构分析证实了2、3、4和5的组成。 [参考:41]

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