Digitale Medien
Weinheim
:
Wiley-Blackwell
Berichte der deutschen chemischen Gesellschaft
2000 (2000), S. 369-374
ISSN:
1434-1948
Schlagwort(e):
Phosphanylcarbenes
;
Substituent effects
;
Quantum chemical calculations
;
Chemistry
;
General Chemistry
Quelle:
Wiley InterScience Backfile Collection 1832-2000
Thema:
Chemie und Pharmazie
Notizen:
A phosphanyl group exerts much less π-conjugation properties than an amino group. On this basis, corresponding carbene structures exhibit much smaller singlet-triplet energy separations. Of the various structures investigated quantum-chemically the largest singlet-triplet energy separations are predicted for cyclic diphosphanylcarbenes, in which the two functional groups are incorporated into a ring system and the phosphorus atoms are substituted by phosphoraniminato groups. Then the singlet-triplet energy separations become essentially larger than for the Bertrand-type (push-pull) carbenes.
Zusätzliches Material:
1 Ill.
Materialart:
Digitale Medien
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