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Metal substrates for use in SAMs can be produced through physical vapor deposition techniques, electrodeposition or electroless deposition. [1] Thiol or selenium SAMs produced by adsorption from solution are typically made by immersing a substrate into a dilute solution of alkane thiol in ethanol, though many different solvents can be used [1] besides use of pure liquids. [16]
Biphenyl (also known as diphenyl, phenylbenzene, 1,1′-biphenyl, lemonene [4] or BP) is an organic compound that forms colorless crystals. Particularly in older literature, compounds containing the functional group consisting of biphenyl less one hydrogen (the site at which it is attached) may use the prefixes xenyl or diphenylyl .
4-Cyano-4'-pentylbiphenyl is a commonly used nematic liquid crystal with the chemical formula C 18 H 19 N. It frequently goes by the common name 5CB. 5CB was first synthesized by George William Gray , Ken Harrison, and J.A. Nash at the University of Hull in 1972 and at the time it was the first member of the cyanobiphenyls.
4,4'-Dihydroxybiphenyl: ... Dihydroxybiphenyls are synthesized through various organic reactions and are used in the preparation of polyether liquid crystals. [1]
The industrial synthesis of 4,4′-biphenol was developed by Allan Hay in the 1960s. [2] [3] As the direct oxidative coupling of phenol gives a mixture of isomers, [4] [5] 4,4′-biphenol is instead prepared from 2,6-di-tert-butylphenol, where para-coupling is the only possibility. [3]
The suspect in the New Orleans attack that killed 14 people on New Year's Day is believed to have acted alone in a "premeditated and evil act," the FBI has said. The latest information is counter ...
A scanning acoustic microscope (SAM) is a device which uses focused sound to investigate, measure, or image an object (a process called scanning acoustic tomography). It is commonly used in failure analysis and non-destructive evaluation .
The acidity of the methylene group in diphenylmethane is due to the weakness of the (C 6 H 5) 2 CH–H bond, which has a bond dissociation energy of 82 kcal mol −1 (340 kJ mol −1). [5] This is well below the published bond dissociation energies for comparable C–H bonds in propane , where BDE((CH 3 ) 2 CH–H)=98.6 kcal mol −1 , and ...