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Theoretical Study on Drum-Shaped Polymers (1,3,5-Triazine) Composed of Nonplanar π-Extended Polymerization Units

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Journal ACS Omega
Specialty Chemistry
Date 2020 Jun 2
PMID 32478252
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Abstract

A nonplanar extended π-system can be found not only in compounds formed by multiple -fused benzenes, such as helicenes and corannulenes, but also in compounds formed by bonding of atoms on the large π-extended rings. (1,3,5-Triazine) ( ≥ 3) are the latter type of compounds that are characterized by monomer units composed entirely of a 1,3,5-triazine core (general formula: CN). The first seven polymers (CN) ( = 3-9) with a drum shape were investigated computationally. Analyses of natural bonding orbitals and atoms in molecules were applied to investigate the bonding properties. In contrast to the planar structure of the 1,3,5-triazine core, the monomer units in (CN) ( = 3-9) are transformed from their planar π-system to a warped one. Similar to properties of the nonplanar π-system in []helicenes and corannulenes, the nonplanar heterocyclic aromatic configuration of the polymerization units is the determinant of the physical and chemical properties of these polymers. The discovery of nonplanar heterocyclic aromatic structures opens up a broad prospect for the study of azacyclic compounds. The results will be the supplement to the study of heterocyclic helicenes and corannulenes.

References
1.
Kruse H, Goerigk L, Grimme S . Why the standard B3LYP/6-31G* model chemistry should not be used in DFT calculations of molecular thermochemistry: understanding and correcting the problem. J Org Chem. 2012; 77(23):10824-34. DOI: 10.1021/jo302156p. View

2.
Brandt J, Wang X, Yang Y, Campbell A, Fuchter M . Circularly Polarized Phosphorescent Electroluminescence with a High Dissymmetry Factor from PHOLEDs Based on a Platinahelicene. J Am Chem Soc. 2016; 138(31):9743-6. DOI: 10.1021/jacs.6b02463. View

3.
Tsefrikas V, Scott L . Geodesic polyarenes by flash vacuum pyrolysis. Chem Rev. 2006; 106(12):4868-84. DOI: 10.1021/cr050553y. View

4.
Schweinfurth D, Zalibera M, Kathan M, Shen C, Mazzolini M, Trapp N . Helicene quinones: redox-triggered chiroptical switching and chiral recognition of the semiquinone radical anion lithium salt by electron nuclear double resonance spectroscopy. J Am Chem Soc. 2014; 136(37):13045-52. DOI: 10.1021/ja5069323. View

5.
Ichinose W, Ito J, Yamaguchi M . Tetrameric ααββ aggregate formation by stereoisomeric bidomain helicene oligomers. Angew Chem Int Ed Engl. 2013; 52(20):5290-4. DOI: 10.1002/anie.201301463. View