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π-Hydrogen bonding and aromaticity: a systematic interplay study.
Physical Chemistry, Chemical Physics - PCCP, 2019Quantum DFT calculations, corrected for long-range interactions, have been carried out on complex models formed between HF as a proton donor and 2-methylene-2H-indene derivatives as proton acceptors.
A. Nekoei, M. Vatanparast
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Polynuclear aromatic hydrocarbons
Environmental Science & Technology, 1981Polynuclear aromatic hydrocarbons (PAHs) can enter the environment in several ways, primarily through the incomplete combustion of carbonaceous materials or through processes that convert coal into synthetic fuels. Other sources of PAHs include the manufacture of carbon black, creosote, soot, vehicular emissions (especially diesel), residual oil, and ...
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Aromaticity and Electrophilic Aromatic Substitution
1977The meaning of the word aromaticity has evolved as understanding of the reason for the special properties of benzene and other aromatic molecules has deepened. Originally, aromaticity was associated with a special chemical reactivity.1 The aromatic hydrocarbons were considered to be those unsaturated systems that underwent substitution reactions in ...
Francis A. Carey, Richard J. Sundberg
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3D global aromaticity in a fully conjugated diradicaloid cage at different oxidation states
Nature Chemistry, 2020Y. Ni +9 more
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Nucleus-Independent Chemical Shifts: A Simple and Efficient Aromaticity Probe.
Journal of the American Chemical Society, 1996P. Schleyer +4 more
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Nucleus-independent chemical shifts (NICS) as an aromaticity criterion.
Chemical Reviews, 2005Zhongfang Chen +4 more
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Aromatic Metamorphosis: Skeletal Editing of Aromatic Rings
Accounts of Chemical ResearchConspectusAromatic rings are fundamental structural motifs found in natural products, synthetic intermediates, pharmaceuticals, agrochemicals, and functional materials. While transformations at the periphery of these rings are well-established, modifying their core frameworks has remained an underexplored frontier.
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Chemistry of meso-Aryl-Substituted Expanded Porphyrins: Aromaticity and Molecular Twist.
Chemical Reviews, 2017Takayuki Tanaka, A. Osuka
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