cyanate

(redirected from Cyanates)
Also found in: Medical, Encyclopedia.

cy·a·nate

 (sī′ə-nāt′, -nət)
n.
The anionic univalent OCN group derived from cyanic acid, or a compound containing this group.
American Heritage® Dictionary of the English Language, Fifth Edition. Copyright © 2016 by Houghton Mifflin Harcourt Publishing Company. Published by Houghton Mifflin Harcourt Publishing Company. All rights reserved.

cyanate

(ˈsaɪəˌneɪt)
n
(Elements & Compounds) any salt or ester of cyanic acid, containing the ion OCN or the group –OCN
Collins English Dictionary – Complete and Unabridged, 12th Edition 2014 © HarperCollins Publishers 1991, 1994, 1998, 2000, 2003, 2006, 2007, 2009, 2011, 2014

cy•a•nate

(ˈsaɪ əˌneɪt, -nɪt)

n.
a salt or ester of cyanic acid.
[1835–45]
Random House Kernerman Webster's College Dictionary, © 2010 K Dictionaries Ltd. Copyright 2005, 1997, 1991 by Random House, Inc. All rights reserved.
Translations
References in periodicals archive ?
These compounds or phytochemical constituents incorporate terpenes, flavonoid, bioflavonoid, benzophenones, xanthenes and also a few metabolites, for example, tannins, saponins, cyanates, oxalate and anthrax-quinones [6].
Therefore a distinction between free, WAD and total cyanide forms (other compounds such as cyanates or thiocyanates are also present) in tailings water is useful for legal regulatory purposes [8].
H., Sushada, C., and Swapan, C., 2008, "A Versatile Series of Nickel(II) Complexes derived from Tetradentate Imine/Pyridyl Ligands and Various Pseudohalides: Azides and Cyanates Compared," Inorganic Chemistry, 47, 10, pp 4109-4117.
All substances were classified in respective chemical groups as: Aliphatic hydrocarbons; aromatic hydrocarbons; isothio cyanates; ketones; nitrosamines; thiazoles; aldehydes; amines; and sulfur compounds.
Aromatic cyanates are low viscosity resins that can crosslink to form polycyanurate networks by forming thermally stable cyclic triazine rings.
Among these materials, thermosetting epoxy resins, polyimides, and cyanate esters were extensively investigated together with fiber-reinforced composites [1].
Cyanate ester (CE) resins have received considerable attention in the past few years because of their importance as thermosetting resins for use in the aerospace, electronics, and adhesive industries [1-6].
A new cyanate ester resin system, EX-1515, from Bryte Technologies, Milpitas, Calif., is said to be unique in that it can achieve an extremely high level of conversion after a 250 F cure.
Structural characterizations reveal that the plasma polymerization of three cyanate ester monomers proceeded mainly via the opening of [pi]-bonds of the cyanate ester functional groups and transforming them to a large [pi]-conjugated structure, which is noticeably different from the conventional thermal or catalytic cyclo-trimerization reaction of cyanate ester monomers.