A complex between ammonia and chlorine studied at 20°K in a nitrogen matrix
✍ Scribed by Göran Ribbeg»rd
- Publisher
- Elsevier Science
- Year
- 1974
- Tongue
- English
- Weight
- 470 KB
- Volume
- 25
- Category
- Article
- ISSN
- 0009-2614
No coin nor oath required. For personal study only.
✦ Synopsis
UV and IR spectra of ammonia and chlorine codeposited in a nitrogen matrix at 20°K have been recorded. An intense absorption band round 2500 A has been observed. An IR-active chlorine stretch frequency of about 460 cm-' and small shifts on the ammonia absorptions were determined. The results are discussed in terms of a charge transfer complex between ammonia and chlorine. From the complex shifts for ammonia and ammonIaA an opening up of the HNH-bond angle on complexing by about 3.6O has been calculated.
. .
📜 SIMILAR VOLUMES
Spectral holes have been burnt in the S, Go O-O transition of resorufin in polymethylmethacrylate (PMMA) and glycerol, and of free-base porphin (H,P) in PMMA and polyethylene (PE). The holewidths follow a T 'J dependence over almost two orders of magnitude in temperature and extrapolate to the fluor
A member of the series M(I)M(III)(ND 3 ) 6 (ClO 4 ) 2 X 2 , CsCo(ND 3 ) 6 (ClO 4 ) 2 Cl 2 , has been examined by single crystal time-of-6ight neutron di4raction at 20, T c ؊10, T c ؉10, and 290 K, adding to previous X-ray di4raction studies of some compounds in this series. T c is the phase transiti
## Abstract To understand the cation–π interaction in aromatic amino acids and peptides, the binding of M^+^ (where M^+^ = Li^+^, Na^+^, and K^+^) to phenylalanine (Phe) is studied at the best level of density functional theory reported so far. The different modes of M^+^ binding show the same orde