We report high-resolution infrared vibrational-rotational spectra of the weakly bound complexes N 2 O-H 2 O and N 2 O-D 2 O in the higher frequency N 2 O stretching mode region (Ξ½ 3 = 2223.756693(124) cm -1 ). The measurements were carried out using a free jet expansion in combination with a lead sa
A High Resolution IR Study of the van der Waals Complexes of HCCCN with CO2and N2
β Scribed by X. Yang; R.Z. Pearson; G. Scoles
- Publisher
- Elsevier Science
- Year
- 1996
- Tongue
- English
- Weight
- 177 KB
- Volume
- 180
- Category
- Article
- ISSN
- 0022-2852
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β¦ Synopsis
The high resolution IR spectra of HCCCN-CO 2 and HCCCN-N 2 have been studied using molecular beam optothermal spectroscopy. For both complexes, structural information has been obtained; HCCCN-CO 2 has been determined to be T-shaped with the CO 2 molecule at the N end of HCCCN, while N 2 -HCCCN was found to be hydrogenbonded in a linear configuration. Accurate molecular constants have been obtained. From the rotational constants, the van der Waals bond lengths of the two dimers have been determined assuming that the structure of the monomer units does not change upon complexation. The results are compared with those for the corresponding complexes of HCN.
π SIMILAR VOLUMES
The weakly bound van der Waals complex CO-N 2 O has been studied for the first time. Absorption spectra in the CO stretching region near 2150 cm 01 were recorded using a tunable diode laser spectrometer to probe the continuous supersonic jet from a slit-shaped nozzle. A total of 186 lines were measu
Rotational spectra of six isotopomers of the van der Waals dimer Ne-N 2 O, namely 20 Ne-14 N 14 NO, 22 Ne-14 N 14 NO, 20 Ne-14 N 15 NO, 22 Ne-14 N 15 NO, 20 Ne-15 N 14 NO, and 22 Ne-15 N 14 NO, were measured in the frequency range between 5 and 18 GHz using a pulsed beam cavity Fourier transform mic
## Abstract For Abstract see ChemInform Abstract in Full Text.
The proton (H) attached to the bold structure at the nitrogen atom of the acylthiourea ligand in Scheme 2 in the printed paper [1] was present in error. These ligands are actually deprotonated, and the proton (H) has been removed in the corrected Scheme 2 shown in this document.