## Abstract The enthalpy change of the complexation reactions of the firstβrow transitional metal chlorides including CrCl~3~, MnCl~2~, FeCl~2~, CoCl~2~, NiCl~2~ and CuCl~2~ with LβΞ±βhistidine in water were determined by a microcalorimeter at 298.15β323.15 K. The standard enthalpy of formation of C
Solid-state complexes of poly(L-histidine) with metal chlorides from the first row of the d-block
β Scribed by Mary Pat McCurdie; Laurence A. Belfiore
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 169 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0887-6266
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β¦ Synopsis
Solid-state characterization of poly(L-histidine) was obtained via differential scanning calorimetry, thermogravimetric analysis, optical microscopy, and infrared spectroscopy. The glass transition temperature of poly(L-histidine) is 169Β°C. This thermal transition has not been reported previously. Poly(L-histidine)'s T g increases when complexes are produced with the following divalent transition metal chlorides: cobalt chloride hexahydrate, nickel chloride hexahydrate, copper chloride dihydrate, and anhydrous zinc chloride. At 10 mol % salt, nickel chloride increases T g by 69Β°C. The enhancement in poly(L-histidine)'s T g correlates well with ligand field stabilization energies for pseudo-octahedral d n complexes (n Ο 7, 8, and 10) from the first row of the d-block. However, d 9 copper(II) complexes do not conform to this empirical correlation. Infrared spectroscopic evidence indicates that these metal chlorides form complexes with the imidazole ring in the histidine side group and the amide group in the main chain of the polymer.
π SIMILAR VOLUMES
Scalar spin-spin coupling constants of some organomanganese complexes, were evaluated by Mn(CO) 5-n (R)L n , lineshape analysis from 13C and 31P solution NMR spectra and from solid-state magic angle spinning spectra showing Γrst-order splitting. Consistent results were obtained for favourable comple