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Monomere und dimere 1,3‐Diaza‐2‐phosphaallyllithium‐Komplexe: Strukturen und ambidente Reaktivität
Author(s) -
Detsch Ralph,
Niecke Edgar,
Nieger Martin,
Schoeller Wolfgang W.
Publication year - 1992
Publication title -
chemische berichte
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.667
H-Index - 136
eISSN - 1099-0682
pISSN - 0009-2940
DOI - 10.1002/cber.19921250522
Subject(s) - chemistry , dimer , reactivity (psychology) , monomer , crystal structure , ether , medicinal chemistry , stereochemistry , polymer chemistry , crystallography , organic chemistry , polymer , medicine , alternative medicine , pathology
Monomer and Dimer 1,3‐Diaza‐2‐phosphaallyllithium Complexes: Structures and Ambident Reactivity * Metallation of the NH‐functional amino(imino)phosphanes Mes * NPNHR (R = CPh 3 , Ad, t Bu) 1a–c yields the 1,3‐diaza‐2‐phosphaallyllithium compounds 2a–c . The crystal structure shows an ether‐stabilized monomer of 2a and a solvent‐free dimer with an eight‐membered ring in the case of 2b, c . The reaction of 2b with chlorodiphenylphosphane yields, dependent on the reaction conditions, (phosphanylamino)iminophosphane 3 or bis(imino)phosphanylphosphorane 4 . The structural and reactivity is discussed on the basis of ab initio calculations.

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