Abstract
Spectra observed, under certain conditions of temperature, pressure, and absorption path, between rotation–vibration lines of the fundamental band of HCl, either pure or mixed with DCl, HBr, DBr, or HI, can be assigned either to the dimer (HCl)2 or to the molecular complexes HCl—DCl, HCl—HBr, HCl—DBr or HCl—HI. The nature of the observed spectra, along with calculations of the energy of interaction between two associated molecules and of the shifts in the spectra of associated HCl vibrators allow us to propose models that correspond, for (HCl)2 and HCl—DCl, to 'orthogonal' and 'antiparallel' configuration, and only to 'orthogonal' configurations for the other complexes.[Journal translation]

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