Aminophosphonium salts [Ph3PN(H)R]BPh4 (1) [R = C6H5CH2 (1a), 4-CH3C 6H4CH2 (1b), C6H5 (1c)] were obtained by allowing hydride IrHCl2(PPh3) 2{P(OEt)3} to react first with triflic acid and then with the organic azide RN3. The compounds were characterized spectroscopically and by X-ray crystal structure determination of [Ph 3PN(H)CH2C6H4-4-CH 3]BPh4 (1b). A reaction path for the formation of aminophosphonium cations is also proposed. © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Aminophosphonium salts [Ph3PN(H)R]BPh4 (1) [R = C6H5CH2 (1a), 4-CH3C6H4CH2 (1b), C6H5 (1c)] were obtained by allowing hydride IrHCl2(PPh3)2{P(OEt)3} to react first with triflic acid and then with the organic azide RN3. The compounds were characterized spectroscopically and by X-ray crystal structure determination of [Ph3PN(H)CH2C6H4-4-CH3]BPh4 (1b). A reaction path for the formation of aminophosphonium cations is also proposed.

Reactions of IrHCl2(PPh3)2{P(OEt)3} with Organic Azides: Formation of Aminophosphonium Salts

ALBERTIN, Gabriele;ANTONIUTTI, Stefano;
2014-01-01

Abstract

Aminophosphonium salts [Ph3PN(H)R]BPh4 (1) [R = C6H5CH2 (1a), 4-CH3C6H4CH2 (1b), C6H5 (1c)] were obtained by allowing hydride IrHCl2(PPh3)2{P(OEt)3} to react first with triflic acid and then with the organic azide RN3. The compounds were characterized spectroscopically and by X-ray crystal structure determination of [Ph3PN(H)CH2C6H4-4-CH3]BPh4 (1b). A reaction path for the formation of aminophosphonium cations is also proposed.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10278/39975
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