Studies in stereochemistry I Steric strains as a factor in the relative stability of some coordination compounds of boron
Studies in stereochemistry I Steric strains as a factor in the relative stability of some coordination compounds of boron
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DOI:
10.1021/ja01254a031
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发表时间:
1942-01-01
影响因子:
15
通讯作者:
Cardon, SZ
中科院分区:
文献类型:
--
作者:
Brown, HC;Schlesinger, HI;Cardon, SZ
Reaction proceeds to right: R= CHS<(CHS) 2CH<(CH3) 3C. investigators to isolate compounds, the isomerism of which is caused by restrictedrotation. 2 Within recent years, the original concept of free rotation has re-quired considerable modification. Not only have instances been dis-covered in the diphenyl3 and ben-zene4 series of isomerism caused by hindered rotation, but also entropy measurements, 5 dipole-moment6 and electron-diffraction7 studies have indicated that rotation in ethane and its simple derivatives is not entirely “free.” The actual isolation of “rotation isomers” in the simple aliphatic derivatives has probably been unsuccessful hitherto only because of the low energy barrier between the iso-meric forms.