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Infrared studies of hydrogen bonding...
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Robertson, William Henry.
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Infrared studies of hydrogen bonding in the presence of negative ions.
紀錄類型:
書目-電子資源 : Monograph/item
正題名/作者:
Infrared studies of hydrogen bonding in the presence of negative ions./
作者:
Robertson, William Henry.
面頁冊數:
228 p.
附註:
Source: Dissertation Abstracts International, Volume: 64-10, Section: B, page: 4963.
Contained By:
Dissertation Abstracts International64-10B.
標題:
Chemistry, Physical. -
電子資源:
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3109453
Infrared studies of hydrogen bonding in the presence of negative ions.
Robertson, William Henry.
Infrared studies of hydrogen bonding in the presence of negative ions.
- 228 p.
Source: Dissertation Abstracts International, Volume: 64-10, Section: B, page: 4963.
Thesis (Ph.D.)--Yale University, 2003.
This thesis is an investigation of the hydration structures formed in the immediate vicinity of anions. Infrared spectroscopy of mass-selected anion hydrate clusters was employed to strip away the contribution of the bulk solvent so as to focus on the molecular details of the highly distorted molecules near the anion. The anionic H-bond was studied by comparing the spectra of several binary anion-water complexes to assess the relative contributions of proton transfer versus electrostatic interactions and the effects of charge delocalization both within molecular anions and away onto competing solvent molecules. These concepts were then exploited in the exploration of water network formation on molecular anions in the higher hydrates. This work provides definitive spectroscopic evidence for hydration shell closure in OH -·(H2O)3 and F-·(H 2O)4 clusters.Subjects--Topical Terms:
560527
Chemistry, Physical.
Infrared studies of hydrogen bonding in the presence of negative ions.
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This thesis is an investigation of the hydration structures formed in the immediate vicinity of anions. Infrared spectroscopy of mass-selected anion hydrate clusters was employed to strip away the contribution of the bulk solvent so as to focus on the molecular details of the highly distorted molecules near the anion. The anionic H-bond was studied by comparing the spectra of several binary anion-water complexes to assess the relative contributions of proton transfer versus electrostatic interactions and the effects of charge delocalization both within molecular anions and away onto competing solvent molecules. These concepts were then exploited in the exploration of water network formation on molecular anions in the higher hydrates. This work provides definitive spectroscopic evidence for hydration shell closure in OH -·(H2O)3 and F-·(H 2O)4 clusters.
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http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3109453
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