New cationic trialkylphosphines [P(CH2NH2R){CH2N(R)CH2N(R)CH2}]+ (R ) C6H5CH2, a; 4-FC6H4CH2, b), as their
Cl- (1a, 1b), SbF6
- (2a, 2b), and PF6
- (3a, 3b) salts, are described. The phosphine framework is conformationally
locked, in the solid state, through pairs of intramolecular N-H · · · N hydrogen bonds which are maintained in the
RuII and RhIII complexes 4 and 5. Phosphines 1a-3b can be considered as charged variants of the well-known
PTA ligand.
Funding
We thank the EPSRC, Loughborough
University, and Niger Delta University, Bayelsa State,
Nigeria, for funding (A.T.E., A.J.L.). Rhodia UK Ltd. (Dr.
Ranbir Padda) and Johnson Matthey are gratefully acknowledged
for their kind donations of THPC and precious metal
salts, respectively. We wish to acknowledge the use of the
EPSRC Chemical Database Service at Daresbury.
History
School
Science
Department
Chemistry
Published in
INORGANIC CHEMISTRY
Volume
48
Issue
6
Pages
2633 - 2638 (6)
Citation
EKUBO, A.T. ... et al, 2009. Intramolecular hydrogen-bonded tertiary phosphines as 1,3,5-triaza-7-phosphaadamantane (PTA) analogues. Inorganic Chemistry, 48 (6), pp. 2633 - 2638.
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