Photochemistry of Azide Complexes of Gold, Silver, Platinum, and Palladium. Generation of the Metallic State
Author(s) -
Vogler A.,
Quett C.,
Kunkely H.
Publication year - 1988
Publication title -
berichte der bunsengesellschaft für physikalische chemie
Language(s) - English
Resource type - Journals
ISSN - 0005-9021
DOI - 10.1002/bbpc.198800356
Subject(s) - chemistry , azide , palladium , photochemistry , photodissociation , platinum , metal , oxidation state , absorption spectroscopy , transition metal , ligand (biochemistry) , quantum yield , inorganic chemistry , catalysis , organic chemistry , fluorescence , biochemistry , physics , receptor , quantum mechanics
The photochemistry of the following azide complexes in organic solvents has been investigated: [Au(N 3 ) 4 ] − , [Au(N 3 ) 2 ] − , [Ag(PPh 3 ) 2 N 3 ], [Pt(N 3 ) 6 ] 2 , [Pt(N 3 ) 4 ] 2− , [Pd(N 3 ) 4 ] 2− , and [Pd 2 (N 3 ) 6 ] 2− . All complexes underwent a photochemical reduction of the metal and oxidation of azide upon ligand to metal charge transfer excitation. The photolysis of the complexes with the metals in the lower oxidation states (Au(I), Ag(I), Pt(II), Pd(II)) led ultimately to the generation of free metals which form colloids. These colloids were characterized by their absorption spectra which showed the typical plasmon bands in the case of gold and silver. Pt(0) and Pd(0) produced during the photolysis can be intercepted with allyl chloride to form [Pt(π‐allyl)Cl] 4 and [Pd(π‐allyl)Cl] 2 . Most photoreactions took place with rather large quantum yields.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom