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首页> 外文期刊>The Journal of Chemical Physics >Pressure and temperature effects on H-2 spin-lattice relaxation times and H-1 chemical shifts in tert-butyl alcohol- and urea-D2O solutions
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Pressure and temperature effects on H-2 spin-lattice relaxation times and H-1 chemical shifts in tert-butyl alcohol- and urea-D2O solutions

机译:压力和温度对叔丁醇和尿素D2O溶液中H-2自旋晶格弛豫时间和H-1化学位移的影响

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The pressure and temperature effects of hydrophobic hydration were studied by NMR spectroscopy, The H-1 chemical shifts (delta) were measured 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 alcohol (TBA)-D2O, and 1 mol kg(-1) urea-D2O solutions, for the methyl group 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 measurements 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 pressure 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)! The decrement of the rotational correlation time of water in the hydration shell of TEA (tau(c)(s),) relative to the value at atmospheric pressure is smaller than that in the bulk (tau(c)(0)). (3) The pressure coefficients of T-1 are positive in dilute solutions but are negative: in more than 4 to 5 mol% solutions, These results suggest that the hydrophobic hydration shell of TEA is different than the open structure of water present in bulk, and resists pressure more strongly than the open structure of water in the bulk, Ln solutions of 4 to 5 mol%, the hydration shell collapses, On the other hand. the tau(c)(s) in the hydration 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 water structure slightly rather than weaken it, although: delta (HDO) approaches that in the hulk with pressure, It is difficult to classify urea into a structure maker or a breaker, (C) 1998 American Institute of Physics. [S0021-9606(98)50604-4] . [References: 38]
机译:通过NMR光谱研究了疏水水合的压力和温度效应,在高至294()MPa的高压下,纯净杂质HDO的H-1化学位移(δ)在7.7、29.9和48.4摄氏度下测量D2O,1 mol kg(-1)叔丁醇(TBA)-D2O和1 mol kg(-1)脲-D2O溶液,TBA-D2O溶液中TEA的甲基和氨基尿素-D2O溶液中的尿素组。 H-2自旋晶格弛豫时间(T-1)在与有机物含量最高为8 mol%的纯D2O,TBA-D2O和尿素-D2O溶液中D2O的化学位移测量相同的条件下测量,以下在TBA-D2O溶液中观察到了对δ(HDO)和H-2-T-1的压力效应的特征:(1)δ(HDO)相对于纯D2O表现出下场偏移,并且TEA溶液与纯净D?O-2之间的差值(HDO)随着增大而变大;较低温度下的压力。 (2)!相对于大气压下的值,TEA水化壳中水的旋转相关时间(tau(c)(s),)的减小量要小于大头中的水(tau(c)(0))的减小。 (3)T-1的压力系数在稀溶液中为正,但为负:在4至5 mol%的溶液中,这些结果表明TEA的疏水水合壳不同于散装水中存在的开放结构另一方面,与体积较大的水的开放结构相比,Ln溶液的耐压性更高(4至5 mol%的Ln溶液会破坏水合壳)。尿素水合壳中的tau(c)在低压下比散装水中的tau(c)稍大,但在高压下明显更大。从水分子的旋转运动来看,尿素似乎会稍微增强水结构而不是削弱水结构,尽管:δ(HDO)在压力下接近绿巨人,很难将尿素分类为结构制造者或破坏者,(C)1998美国物理研究所。 [S0021-9606(98)50604-4]。 [参考:38]

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