PRESSURE AND TEMPERATURE EFFECTS ON H-2 SPIN-LATTICE RELAXATION-TIMESAND H-1 CHEMICAL-SHIFTS IN TERT-BUTYL ALCOHOL-D2O AND UREA-D2O SOLUTIONS

Citation
K. Yoshida et al., PRESSURE AND TEMPERATURE EFFECTS ON H-2 SPIN-LATTICE RELAXATION-TIMESAND H-1 CHEMICAL-SHIFTS IN TERT-BUTYL ALCOHOL-D2O AND UREA-D2O SOLUTIONS, The Journal of chemical physics, 108(4), 1998, pp. 1360-1367
Citations number
38
Categorie Soggetti
Physics, Atomic, Molecular & Chemical
ISSN journal
00219606
Volume
108
Issue
4
Year of publication
1998
Pages
1360 - 1367
Database
ISI
SICI code
0021-9606(1998)108:4<1360:PATEOH>2.0.ZU;2-P
Abstract
The pressure and temperature effects of hydrophobic hydration were stu died by NMR spectroscopy, The H-1 chemical shifts (delta) were measure d at 7.7, 29.9, and 48.4 degrees C under high pressure up to 294() MPa for HDO contained as impurity in neat D2O, 1 mol kg(-1) tert-butyl al cohol (TBA)-D2O, and 1 mol kg(-1) urea-D2O solutions, for the methyl g roup of, TEA in the TBA-D2O solution, and for the amino group of urea in the urea-D2O solution. The H-2 spin-lattice relaxation times (T-1) were measured under the same conditions as the chemical shift measurem ents for D2O in neat D2O, TBA-D2O and urea-D2O solutions with organic contents up to 8 mol%, The following features are observed for the pre ssure effect on delta (HDO) and H-2-T-1 in TBA-D2O solutions: (1) The delta (HDO) ,exhibits a downfield shift relative to that in neat D2O, and the difference of delta (HDO) between TEA solution and neat D?O-2 becomes larger with increasing; pressure at lower temperature. (2)! Th e decrement of the rotational correlation time of water in the hydrati on shell of TEA (tau(c)(s),) relative to the value at atmospheric pres sure is smaller than that in the bulk (tau(c)(0)). (3) The pressure co efficients of T-1 are positive in dilute solutions but are negative: i n more than 4 to 5 mol% solutions, These results suggest that the hydr ophobic hydration shell of TEA is different than the open structure of water present in bulk, and resists pressure more strongly than the op en structure of water in the bulk, Ln solutions of 4 to 5 mol%, the hy dration shell collapses, On the other hand. the tau(c)(s) in the hydra tion shell of urea is slightly larger than that in bulk water at lower pressure, but is obviously larger at higher pressure. Ln view of the rotational motion of water molecules, urea seems to strengthen the wat er structure slightly rather than weaken it, although: delta (HDO) app roaches that in the hulk with pressure, It is difficult to classify ur ea into a structure maker or a breaker, (C) 1998 American Institute of Physics. [S0021-9606(98)50604-4] .