Sn( ii )–carbon bond reactivity: radical generation and consumption via reactions of a stannylene with alkynes
Sn( ii )–carbon bond reactivity: radical generation and consumption via reactions of a stannylene with alkynes
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Sn( ii )–碳键反应性:通过亚锡与炔烃的反应产生自由基和消耗自由基
DOI:
10.1039/d3cc04014c
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发表时间:
2023
影响因子:
4.9
通讯作者:
Power, Philip P.
中科院分区:
文献类型:
--
作者:
Zou, Wenxing;Mears, Kristian L.;Fettinger, James C.;Power, Philip P.
Thermal Sn–C cleavage in the diarylstannylene Sn(AriPr4)2 (AriPr4 = C6H3-2,6-(C6H3-2,6-iPr2)2) was used to generate ˙Sn(AriPr4) and ˙AriPr4 radicals for alkyne arylstannylation. The radical pair and RCCR′ (R = H, R′ = Ph; R = Ph, R′ = Ph; R = H, R′ = C4H9; R = H, R′ = SiMe3) in refluxing benzene generate the aryl vinyl stannylene complexes, AriPr4Sn{C(C6H5)-C(H)(AriPr4)} (1), AriPr4Sn{C(C6H5)-C(H)(C6H5)} (2) and AriPr4Sn{C(C4H9)-C(H)(AriPr4)} (3) respectively. For HCCSiMe3, the known distannene {Sn(CCSiMe3)AriPr4}2 (4) was also generated from this new method.