1996
DOI: 10.1016/s0584-8539(96)01736-9
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Infrared spectroscopy study of cyclopentanol self-associations

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Cited by 6 publications
(16 citation statements)
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“…However, in most studies, the concentration dependent distribution of monomeric and aggregated alcohol is not considered, making it questionable to attach any molecular meaning to the reaction order. Such data are available for cyclopentanol in the solvents used [1].…”
Section: S: H--o-rmentioning
confidence: 99%
“…However, in most studies, the concentration dependent distribution of monomeric and aggregated alcohol is not considered, making it questionable to attach any molecular meaning to the reaction order. Such data are available for cyclopentanol in the solvents used [1].…”
Section: S: H--o-rmentioning
confidence: 99%
“…[14] It has been reported that there were two plastic phases and two ordered crystalline phases below the melting point. [5] According to this result, we can conclude that cyclopentanol shows the first plastic phases (phase I) below the melting point of 254 K. Below 222 K, another plastic phase (phase II) is formed. The first ordered phase (phase III) is found to be stable below the temperature of 206 K. Below 172 K, another crystalline structure, phase IV, is formed.…”
Section: Resultsmentioning
confidence: 66%
“…However, two crystal phases III and IV at lower temperature are completely in order in both position and orientation. [5] Many distinct changes are observed in the spectra, including the band sharpening and new peak appearance. Figure 3 displays the Raman spectrum of cyclopentanol at different pressures.…”
Section: Resultsmentioning
confidence: 99%
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