aromaticity

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ar·o·ma·tic·i·ty

 (ăr′ə-mə-tĭs′ĭ-tē, ə-rō′mə-)
n. pl. ar·o·ma·tic·i·ties
Aromatic quality or character, especially the distinctive structure or properties of the aromatic chemical compounds.
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.

aromaticity

(əˌrəʊməˈtɪsɪtɪ)
n
1. (Chemistry) the property of certain planar cyclic conjugated molecules, esp benzene, of behaving like unsaturated molecules and undergoing substitution reactions rather than addition as a result of delocalization of electrons in the ring
2. the quality or state of having an aroma
Collins English Dictionary – Complete and Unabridged, 12th Edition 2014 © HarperCollins Publishers 1991, 1994, 1998, 2000, 2003, 2006, 2007, 2009, 2011, 2014
Translations
aromaticitet
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References in periodicals archive
The new metal structures show a tantalizing trait called aromaticity. This molecule-stabilizing property was named after the first such molecules identified, including benzene, which have noticeable aromas.
These polymers lacked the highly ordered, stiff backbones of conventional polyimides, and this loss of aromaticity greatly diminished the ability to compete with high performance aromatic polyimides.
Despite that, all HI and PI values were less than one across the sampled treatment combinations (Table 1), implying lower aromaticity of [C.sub.HA].
This difference in pyrolysis among the three [beta] resins was caused by the dissimilarity in their aromaticity index (Iar) and CH3/CH2 ratio; these factors significantly affect the aromaticity and number of aliphatic side chains in [beta] resin.
The higher H/C ratio of the CS-Fe over CS indicated that more original organic matter was preserved in the iron-loaded biochar and showed lower overall aromaticity. The higher O/C ratios of the CS-Fe indicated higher polarity when compared to CS [22].
However, the aromaticity of G1 makes it much more stable than G2, which displays an exocyclic double bond between C(4) and C (15).
Their topics are mathematical chemistry, graph theory and chemistry, characteristic polynomial, structure-activity, molecular descriptors, partial ordering, novel molecular matrices, on highly similar molecules, aromaticity revisited, clar aromatic sextet, renormalization in chemistry, graphical bioinformatics, and beauties and sleeping beauties in science.
This happens in a way that increases in the aromaticity of D-amino bridges and replacing of hydroxyl groups with methoxy (except some items) will lead to increase in anticancer feature [2, 28].
The salicylaldimines exist predominantly in-OH tautomeric form in crystalline state and the reason behind this is the loss of ring aromaticity [26].
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