852242-57-0Relevant articles and documents
Phosphepines: Convenient access to phosphinidene complexes
Borst, Mark L. G.,Bulo, Rosa E.,Winkel, Christiaan W.,Gibney, Daniele J.,Ehlers, Andreas W.,Schakel, Marius,Lutz, Martin,Spek, Anthony L.,Lammertsma, Koop
, p. 5800 - 5801 (2007/10/03)
Reaction of o-diethynylbenzene with transition metal-complexed primary phosphines gives in a single base-induced step stable phosphepine complexes as confirmed by X-ray data. At 75-80 °C these phosphepines undergo clean cheletropic elimination of naphthalene to give transient carbene-like phosphinidene complexes that can be trapped in high yield by alkenes, alkynes, and alcohols. Copyright
3H-benzophosphepine complexes: Versatile phosphinidene precursors
Borst, Mark L. G.,Bulo, Rosa E.,Gibney, Daniele J.,Alem, Yonathan,De Kanter, Frans J. J.,Ehlers, Andreas W.,Schakel, Marius,Lutz, Martin,Spek, Anthony L.,Lammertsma, Koop
, p. 16985 - 16999 (2007/10/03)
The synthesis of a variety of benzophosphepine complexes [R = Ph, t-Bu, Me; MLn = W(CO)5, Mo(CO)5, Cr(CO)5, Mn(CO)2Cp] by two successive hydrophosphinations of 1,2-diethynylbenzene is discussed in det