Interpretation of Both Electron Pushing and Electron Withdrawing Inductive Effect of Alkyl Groups in Terms of Mulliken-Jaffe’s Charge Coefficient Parameters (b)
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DOI: 10.1007/s12045-019-0798-0
Abstract: Alkyl groups can delocalize both the negative and positive charges through ion (charge)-induced dipole interaction with the polarizable alkyl groups. This charge induced polarization of the alkyl group to delocalize the charge is the origin… read more here.
Keywords: alkyl; inductive effect; effect alkyl; charge ... See more keywords
β-Hexaalkylporphycenes: Positional Effect of Alkyl Groups toward Design and Control of Structural and Photophysical Properties in Isomeric Hexaethylporphycenes.
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DOI: 10.1021/acs.orglett.6b03428
Abstract: Two novel β-hexaalkylated porphycenes, i.e., 2,3,7,12,13,17- (HOT) and 2,3,6,12,13,16-hexaethylporphycenes (HIT) were introduced for the first time in porphycene chemistry. These were synthesized through McMurry coupling reactions of new isomeric unsymmetrically substituted triethylbipyrrole dialdehydes. The positional… read more here.
Keywords: effect alkyl; hexaalkylporphycenes positional; positional effect; groups toward ... See more keywords
Figure-eight thermal hysteresis of aminomethylenehelicene oligomers with terminal C16 alkyl groups during hetero-double-helix formation†
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DOI: 10.1039/c9sc06496f
Abstract: 1 : 1 mixtures of aminomethylenehelicene (P)-tetramer and (M)-pentamer with terminal C16 alkyl groups in fluorobenzene showed structural changes between hetero-double-helices B and C and random-coils 2A. Figure-eight thermal hysteresis appeared when the solution was cooled and… read more here.
Keywords: terminal c16; c16 alkyl; thermal hysteresis; alkyl groups ... See more keywords