Sm. Barnett et al., PRESSURE-TUNING INFRARED AND SOLUTION RAMAN-SPECTROSCOPIC STUDIES OF 17-BETA-ESTRADIOL AND SEVERAL A-RING AND 17-ALPHA-ETHYNYLESTRADIOL DERIVATIVES, Vibrational spectroscopy, 8(2), 1995, pp. 263-277
The vibrational spectrum of the hormonal steriod (17)beta-estradiol ha
s been assigned with the aid of pressure-tuning infrared (IR) and solu
tion Raman spectroscopy. In addition, a pressure-tuning IR study of 17
alpha-ethynylestradiol suggests that the 17 alpha-ethynyl hydrogen is
hydrogen bonded in the solid state. Related work on a series of organ
ometallic estradiol derivatives indicates that the effect of substitut
ion chiefly affects the pressure sensitivities of vibrational modes lo
cated near the point of substitution. For the alpha- and beta-[Cr(CO)(
3)]-17 beta-estradiol diastereomers, several vibrational spectroscopic
differences were noted and the alpha-[Cr(CO)(3)] fragment apparently
has a steric effect on the extent of hydrogen bonding.