Literature DB >> 12418903

A theoretical and experimental scale of aromaticity. The first nucleus-independent chemical shifts (NICS) study of the dimethyldihydropyrene nucleus.

Richard Vaughan Williams1, John R Armantrout, Brendan Twamley, Reginald H Mitchell, Timothy R Ward, Subhajit Bandyopadhyay.   

Abstract

Nucleus-independent chemical shift (NICS) values were calculated at several locations for a series of dimethyldihydropyrenes (DDPs). These NICS values were used to assess the relative aromaticities of the dimethyldihydropyrene nucleus (DDPN) of these DDPs and to construct a NICS scale of aromaticity. The NICS and experimentally determined relative aromaticities of these DDPNs are in complete agreement, verifying that NICS can be used not only to classify a compound as aromatic but also to determine the degrees of aromaticity of structurally related systems.

Entities:  

Year:  2002        PMID: 12418903     DOI: 10.1021/ja020595t

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  2 in total

1.  Influence of quantum dots on the aromaticity of thiosalicylic acid.

Authors:  Qiumei Guan
Journal:  J Mol Model       Date:  2013-08-11       Impact factor: 1.810

Review 2.  Charge-Transfer Interactions in Organic Functional Materials.

Authors:  Hsin-Chieh Lin; Bih-Yaw Jin
Journal:  Materials (Basel)       Date:  2010-08-05       Impact factor: 3.623

  2 in total

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