期刊
ORGANOMETALLICS
卷 30, 期 11, 页码 2986-2992出版社
AMER CHEMICAL SOC
DOI: 10.1021/om200092y
关键词
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资金
- Swiss National Science Foundation
- University of Zurich
A series of [ReBr2(MeCN)(NO)(P boolean AND P)] complexes (P boolean AND P = 1,1'-bis(diphenylphosphino)ferrocene (dppfc) (1a), 1,1'-bis(diisopropylphosphino)ferrocene (diprpfc) (1b), 2,2'-bis(diphenylphosphino)diphenyl ether (dpephos) (1c), 10,11-dihydro-4,5-bis(diphenylphosphino)dibenzo[b,f]oxepine (homoxantphos) (1d), 4,6-bis(diphenylphosphino)-10,10-dimethylphenoxasilin (Sixantphos) (1e)) were prepared with diphosphines varying in the P-Re-P bite angles. 1a,c-e were obtained from the reaction of [ReBr5(NO)][NEt4](2) with an an excess of the respective diphosphine in MeCN or MeCN/THF mixtures at elevated temperatures. Compound 1b was obtained by an alternative route, cleaving the dinuclear [{ReBr(mu(2)-Br)(NO)(diprpfc)1}(2)] unit (2b) with MeCN. 2b was prepared from the reaction of [ReBr5(NO)][NEt4](2) with diprpfc in EtOH. The reaction of 1a-d with HSiEt3 gave the seven-coordinate [ReBr(H)(2)(SiEt3)(NO)(P boolean AND P)] compounds 4a-d, of which 4a,c,d are only stable in solution in the presence of HSiEt3. The SiMe3 (4f) and SiCl3 (4g) derivatives of 4b were also prepared by applying the reaction of lb with HSiMe3 and HSiCl3. 1a,c,e, 2b, and 4f,g were structurally characterized. For 1c,e, 2b, and 4f,g NO/Br disorder was observed, which originates from the presence of two isomeric forms in the crystals of the respective compounds. For lc,d fast interconversion of these isomers could be observed in their P-31{H-1} NMR spectra at room temperature.
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