Geminal dianions stabilized by phosphonium substituents
نویسندگان
چکیده
منابع مشابه
Electrophilic phosphonium cations (EPCs) with perchlorinated-aryl substituents: towards air-stable phosphorus-based Lewis acid catalysts.
A series of phosphines incorporating (C6Cl5) substituents, Ph2P(C6Cl5) 1, PhP(C6Cl5)22, P(C6Cl5)33 and (C6F5)P(C6Cl5)24 were prepared. In the case of 1, 2 and 4, these were converted to the corresponding aryl-difluorophosphoranes 5-7via reaction with XeF2, whereas reaction of 3 with XeF2 afforded only an inseparable mixture of products. The compounds 5-7 were converted to the fluorophosphonium ...
متن کاملAntiaromatic dianions: dianions of dixanthylidene by reduction and attempted excited-state deprotonation.
Reduction of dixanthylidene with potassium or lithium resulted in formation of the antiaromatic dianion in high yield. Attempts to form the dianion by excited-state deprotonation of dixanthene with n-butyllithium/TMEDA resulted in formation of the tetraanion from deprotonation ortho to the oxygen. Orientation of the sp(3) hydrogens presumably allows preferential deprotonation of the xanthene ri...
متن کاملChemistry of a geminal frustrated Lewis pair featuring electron withdrawing C6F5 substituents at both phosphorus and boron.
Hydroboration of the electron poor phosphine (1-propenyl)P(C(6)F(5))(2) with Piers' borane [HB(C(6)F(5))(2)] gave the geminal frustrated Lewis pair (C(6)F(5))(2)P-CH(Et)-B(C(6)F(5))(2). It undergoes 1,2-addition reactions to an alkene and an alkyne and to the C=N bond of an isocyanate. With mesityl azide it undergoes a 1,3-addition reaction.
متن کاملMixed valence/dipole-bound dianions
The possibility of binding two electrons to a molecule utilizing two distinct electron binding sites ~i.e., one valenceand one dipole-binding center! is studied using ab initio electronic structure methods. It is found that if the electron binding energy of the dipole-binding site is large enough to overcome the Coulomb repulsion produced by the valence-bound electron, the dianion can be electr...
متن کاملIntramolecular frustrated lewis pairs: formation and chemical features.
Intramolecular vicinal and geminal frustrated Lewis pairs (FLPs) featuring bulky substituents at phosphorus or nitrogen and strongly electron-withdrawing bulky pentafluorophenyl substituents at boron undergo a variety of addition and/or activation reactions with small molecules. A number of examples of such reactions are presented and discussed, among them the FLP activation of dihydrogen to gi...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Coordination Chemistry Reviews
سال: 2011
ISSN: 0010-8545
DOI: 10.1016/j.ccr.2010.11.021