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INTRA-MOLECULAR EASILY POLARIZABLE HYDROGEN-BONDS IN DIAMIDES OF SUCCINIC AND ORTHO-PHTHALIC ACID
被引:13
作者
:
BRZEZINSKI, B
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV MUNICH,INST PHYS CHEM,D-8000 MUNICH 2,FED REP GER
UNIV MUNICH,INST PHYS CHEM,D-8000 MUNICH 2,FED REP GER
BRZEZINSKI, B
[
1
]
ZUNDEL, G
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV MUNICH,INST PHYS CHEM,D-8000 MUNICH 2,FED REP GER
UNIV MUNICH,INST PHYS CHEM,D-8000 MUNICH 2,FED REP GER
ZUNDEL, G
[
1
]
机构
:
[1]
UNIV MUNICH,INST PHYS CHEM,D-8000 MUNICH 2,FED REP GER
来源
:
CHEMICAL PHYSICS LETTERS
|
1979年
/ 61卷
/ 02期
关键词
:
D O I
:
10.1016/0009-2614(79)80651-X
中图分类号
:
O64 [物理化学(理论化学)、化学物理学];
学科分类号
:
070304 ;
081704 ;
摘要
:
Succinic 1, o-phthalic 2 and oxalic 3 acid diamides (acetonitrile-d3 solutions) as well as their perchlorates were studied by proton magnetic resonance and infrared spectroscopy. With compounds 1 and 2 the protons are added to the N atoms but no intramolecular symmetrical N+H ... N ⇌ N ... H+N hydrogen bonds are formed. The NH+ groups build up intramolecular asymmetrical N+H ... OCN ⇌ N ... HOC+N hydrogen bonds. A double-minimum energy surface is present in these intramolecular bonds. They are easily polarizable. Hydrogen-bonded N+H groups are in equilibrium with non-hydrogen-bonded N+H groupgs. With the perchlorate of oxalic acid diamide 3, the protons are added to the O atoms of carbonyl groups. Most of the O+H groups formed interact only weakly with their environment. However, a few groups form intermolecular structurally symmetrical easily polarizable O+H ... O ⇌ O ... H+O hydrogen bonds. © 1979.
引用
收藏
页码:315 / 318
页数:4
相关论文
共 11 条
[11]
Zundel G, 1976, HYDROGEN BOND RECENT
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共 11 条
[11]
Zundel G, 1976, HYDROGEN BOND RECENT
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1
2
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