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Novel Reactions of Phosphaalkynes in the Coordination Sphere of tert ‐Butylimido‐ vanadium( V ) Complexes: A Simple Synthesis of 3‐Aza‐1,2,4,6‐tetraphosphaquadricyclanes and 1,3,5‐Triphosphabenzenes
Author(s) -
Tabellion Frank,
Nachbauer Anja,
Leininger Stefan,
Peters Christoph,
Preuss Fritz,
Regitz Manfred
Publication year - 1998
Publication title -
angewandte chemie international edition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 1433-7851
DOI - 10.1002/(sici)1521-3773(19980518)37:9<1233::aid-anie1233>3.0.co;2-x
Subject(s) - chemistry , vanadium , reagent , dimethoxyethane , inorganic chemistry , electrode , electrolyte
A small variation in the vanadium reagent leads to a completely different product: The cyclooligomerization of phosphaalkynes 2 with t BuN=VCl 3 ⋅DME (DME=1,2‐dimethoxyethane) proceeds with incorporation of the imido fragment to give the azatetraphosphaquadricyclanes 1 . In contrast, with the corresponding vanadium compound containing no Lewis base this fragment is not incorporated, and the 1,3,5‐triphosphabenzenes 3 are obtained.

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