Results 91 to 100 of about 4,127 (128)
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The Journal of Chemical Thermodynamics, 1974
Abstract Excess enthalpies for cyclopentane+cycloheptane at 288.15, 298.15, and 308.15 K and excess enthalpies for cyclohexane+cyclo-octane at 288.15, 298.15, 308.15, and 318.15 K have been measured with an isothermal displacement calorimeter. The excess volumes for cyclopentane+cyclohexane and cyclopentane+cycloheptane have been measured over a ...
M.B Ewing, K.N Marsh
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Abstract Excess enthalpies for cyclopentane+cycloheptane at 288.15, 298.15, and 308.15 K and excess enthalpies for cyclohexane+cyclo-octane at 288.15, 298.15, 308.15, and 318.15 K have been measured with an isothermal displacement calorimeter. The excess volumes for cyclopentane+cyclohexane and cyclopentane+cycloheptane have been measured over a ...
M.B Ewing, K.N Marsh
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Decomposition of cyclopentane on Ni(755): peculiar decomposition behavior of cyclopentane
Surface Science Letters, 1993Abstract Decomposition of cyclopentane on Ni(755) and −(111) has been investigated by temperature-programmed desorption (TPD). Adsorption of cyclopentane occurs on both surfaces by a precursor-mediated mechanism. On the (755) surface cyclopentane decomposes almost completely into adsorbed carbon and gaseous hydrogen while heating up from 123 to 573 K.
H. Kuramochi +5 more
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Appliance Rigid Foams Blown with Cyclopentane and Cyclopentane/Isopentane Blends
Journal of Cellular Plastics, 2000Since CFC 11 was eliminated from use in rigid foams in the mid 1990s, the blowing agent of choice in North America has primarily been HCFC 141b. In the USA, we are now faced with the phase-out of HCFC 141b by the year 2003. The blowing agent that will replace HCFC 141b must be non-ozone depleting and should also have low thermal conductivity and a low
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The Infra-Red and Raman Spectra of Cyclopentane, Cyclopentane-d1, and Cyclopentane-d10
The Journal of Chemical Physics, 1950The infra-red and Raman spectra of cyclopentane, cyclopentane-d1, and cyclopentane-d10 have been determined for the purpose of establishing the symmetry of cyclopentane. D5h selection rules are found to hold very well. This does not constitute a rigorous criterion for structure in this case, however, because drastic alteration of the symmetry by ...
Foil A. Miller, Richard G. Inskeep
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Diastereoselective Cyclopentane Construction
The Journal of Organic Chemistry, 2000, Taber, , Wang, , Pahutski
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Cyclopentane analog of muscarone
Journal of Medicinal Chemistry, 1974F, Gualtieri +3 more
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Über die thermische Zersetzung von Cyclopentan und Methyl‐cyclopentan
Berichte der deutschen chemischen Gesellschaft (A and B Series), 1934B. A. Kasansky, A. F. Plate
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