Please use this identifier to cite or link to this item:
|Title:||Thermal degradation of transition metal carbonyl complexes. Part II - Thermogravimetry and differential scanning calorimetry of monosubstituted pyridine carbonyls of chromium, molybdenum and tungsten||Authors:||Chan, H.S.O.
|Issue Date:||Jan-1988||Citation:||Chan, H.S.O., Hor, T.S.A., Lusty, J.R., Lim, K.H., Chiam, C.S.M. (1988-01). Thermal degradation of transition metal carbonyl complexes. Part II - Thermogravimetry and differential scanning calorimetry of monosubstituted pyridine carbonyls of chromium, molybdenum and tungsten. Journal of Thermal Analysis 34 (1) : 121-133. ScholarBank@NUS Repository. https://doi.org/10.1007/BF01913379||Abstract:||The thermal degradation of three monosubstituted hexacarbonyl complexes, M(CO)5py (where M=Cr, Mo, and W; py=pyridine) has been studied by thermogravimetry (TG) and differential scanning calorimetry (DSC) and their results reported. It was found that for each of the three complexes studied, the starting material M(CO)6 was formed which immediately sublimed unchanged with or without concomitant loss of carbonyl (CO) ligands to give the first large weight loss step. This was closely followed by the volatilisation of the pyridine ligands and at higher temperatures the loss of further CO ligands. The enthalpy changes associated with the above-mentioned steps are reported. The conversion of M(CO)5py to M(CO)6 and other products was confirmed by the analysis of residue after pyrolysis in a tube furnace under conditions similar to those observed in TG experiments. © 1988 Wiley Heyden Ltd., Chichester and Akadémiai Kiadó, Budapest.||Source Title:||Journal of Thermal Analysis||URI:||http://scholarbank.nus.edu.sg/handle/10635/95290||ISSN:||03684466||DOI:||10.1007/BF01913379|
|Appears in Collections:||Staff Publications|
Show full item record
Files in This Item:
There are no files associated with this item.
checked on Jan 23, 2023
WEB OF SCIENCETM
checked on Jan 16, 2023
checked on Jan 26, 2023
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.