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Vibrational coupling as diagnostic for intramolecular hydrogen bonds of carbohydrates in aqueous solution

机译:振动偶合用于诊断水溶液中碳水化合物的分子内氢键

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摘要

The coupling of vC-O and deltaO-D vibrations in the 1200-900 cm(-1) IR range leads to band shifting in opposite directions, which provides information on intramolecular hydrogen bonding of carbohydrates in aqueous solution. The aqueous solution IR spectra of 2-acetamide-1,6-anhydro-2-deoxy-D-glucopyranose and cis-1,2-cyclopentanediol and tetrahydrofuran-ethanol mixtures are reported. Frequency up-shifting upon deuteration is observed for the vC-O bands of both a hydrogen bond acceptor and donor in ether-hydroxyl and hydroxyl-hydroxyl contacts. The 1200-900 cm(-1) range can be used to reveal the presence of intramolecular hydrogen bonds in aqueous carbohydrates, unlike the OH stretching region, which cannot be used in this sense due to carbohydrate band masking by the strong vOH IR absorption of water. (C) 2002 John Wiley & Sons, Inc. Biopolymers (Biospectroscopy) 67: 20-25, 2002; DOI 10.1002/bip. 10024. [References: 22]
机译:1200-900 cm(-1)IR范围内的vC-O和deltaO-D振动的耦合导致带向相反方向移动,从而提供了水溶液中碳水化合物的分子内氢键合信息。报道了2-乙酰胺-1,6-脱水-2-脱氧-D-吡喃葡萄糖和顺式1,2-环戊二醇与四氢呋喃-乙醇混合物的水溶液红外光谱。在醚-羟基和羟基-羟基接触中,氢键受体和供体的vC-O谱带都在氘化时观察到频率上移。 1200-900 cm(-1)范围可用于揭示水性碳水化合物中分子内氢键的存在,这与OH拉伸区域不同,该区域在这种意义上无法使用,因为碳水化合物被强vOH IR吸收掩盖了水。 (C)2002 John Wiley&Sons,Inc.生物聚合物(Biospectroscopy)67:20-25,2002; DOI 10.1002 / bip。 10024. [参考:22]

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