A general theory is derived for the optical rotatory power of molecules which exhibit this property only on account of isotopic substitution. The optical rotatory power is evaluated from the interaction between the nuclei and the radiation field only, and it is concluded that this is a good approximation for infrared light. Detailed calculations are performed for the molecules CHDBrCl, CCl35Cl37BrF, and CHDTBr. Various summation rules are derived for the vibrational rotatory strengths. © 1966, American Chemical Society. All rights reserved.
Documento: | Artículo |
Título: | Isotope Effects in Optical Rotation |
Autor: | Cohan, N.V.; Hameka, H.F. |
Filiación: | Laboratory for Research on the Structure of Matter, University of Pennsylvania, Philadelphia 4, Pennsylvania., United States Departamento de Quimica Inorganics, Analitica y Fisicoquimica, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Buenos Aires, Argentina, United States |
Año: | 1966 |
Volumen: | 88 |
Número: | 10 |
Página de inicio: | 2136 |
Página de fin: | 2142 |
DOI: | http://dx.doi.org/10.1021/ja00962a010 |
Título revista: | Journal of the American Chemical Society |
Título revista abreviado: | J. Am. Chem. Soc. |
ISSN: | 00027863 |
Registro: | https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00027863_v88_n10_p2136_Cohan |