Department of Chemistry, Graduate School of Engineering Science, Osaka University, Toyonaka, Osaka 560-8531, Japan.
Chem Commun (Camb). 2018 Apr 10;54(30):3709-3711. doi: 10.1039/c7cc08570b.
A metathesis reaction of a W[triple bond, length as m-dash]W bond and an N[double bond, length as m-dash]N bond was observed by reacting a W-W triply-bonded W(iii)2 complex, (tBuO)3W[triple bond, length as m-dash]W(OtBu)3 (1), with benzo[c]cinnoline derivatives to form biphenyl-linked dinuclear (imido)tungsten complexes 2-4. When azobenzene was used as the substrate, a trans to cis isomerization induced by blue-LED light was essential prior to the metathesis cleavage of the N[double bond, length as m-dash]N bond by the W[triple bond, length as m-dash]W bond of (Me2N)2(TfO)W[triple bond, length as m-dash]W(OTf)(NMe2)2 (6), affording the corresponding imido-bridged dinuclear tungsten complexes 7-9.
观察到了 W[三键,长度为破折号]W 键和 N[双键,长度为破折号]N 键的复分解反应,方法是使 W-W 三重键合的 W(iii)2 配合物(tBuO)3W[三键,长度为破折号]W(OtBu)3(1)与苯并[c]咔啉衍生物反应,形成联苯连接的双核(亚氨基)钨配合物 2-4。当使用偶氮苯作为底物时,在 N[双键,长度为破折号]N 键的复分解裂解之前,由 W[三键,长度为破折号]W 键的(Me2N)2(TfO)W[三键,长度为破折号]W(OTf)(NMe2)2(6)引发的反式到顺式的异构化是必需的,得到相应的亚氨基桥联双核钨配合物 7-9。