期刊
ORGANOMETALLICS
卷 28, 期 17, 页码 5183-5190出版社
AMER CHEMICAL SOC
DOI: 10.1021/om900439z
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资金
- National Science Foundation [CHE-0075246, 0647252]
- Division Of Chemistry
- Direct For Mathematical & Physical Scien [0647252] Funding Source: National Science Foundation
Lithium-halogen exchange of (Z)-1,2-diphenyl-3-(2-iodoethenyl)cyclopropene (1) and subsequent addition to (eta(4)-1,5-cod)PtCl2 yields the platinabenzene (eta(C5H3Ph2)-C-5)[PtC5H3Ph2] (7), in which the metallacyclic ring and C5H3Ph2 (CP') unit are both derived from the cyclopropene skeleton. Starting instead with (eta(5)-C5Me5)Pt(CO)I, treatment with three nucleophilic (Z)-3-(2-lithiovinyl)cyclopropenes provides platinabenzenes (eta(5)-C5Me5)[PtC5H3PhR] (R = Ph (8), t-Bu (9), Me (10)) in low to modest yield. All platinaberizenes have been fully characterized by NMR spectroscopy and X-ray crystallography. Intermediate sigma-vinyl complexes (eta(5)-C5Me5)Pt(sigma-C5H3PhR) (R = Ph (14), t-Bu (15)) are also isolated from the reaction mixtures and convert cleanly to the corresponding platinaberizenes in near quantitative yield. Reactivity studies of (eta(5)-C5Me5)[PtC5H3Ph2] with a variety of reagents/conditions are also reported.
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