An aromatic saddle was designed from the hypothetical three-dimensional graphene with the negative Gaussian curvature (Schwarzite P192). Two aromatic saddles, tetrabenzo[8]circulene (TB8C) and its octamethyl derivative OM-TB8C, were synthesized by the Scholl reaction of cyclic octaphenylene precursors. The structure of TB8C greatly deviates from planarity, and the deep saddle shape was confirmed by single-crystal X-ray crystallography. There are two conformers with the S4 symmetry, which are twisted compared to the DFT structure (D2d). The theoretical studies propose that the interconversion of TB8C via the planar transition state (125 kcal mol(-1)) is not possible. However, the pseudorotation leads to a low-energy tub-to-tub inversion via the nonplanar transition state (7.3 kcal mol(-1)). The ground-state structure of TB8C in solution is quite different from the X-ray structure because of the crystal-packing force and low-energy pseudorotation. OM-TB8C is a good electron donor and works as the p-type semiconductor.
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http://dx.doi.org/10.1021/ja407842z | DOI Listing |
J Chem Phys
December 2024
Institute of Atomic and Molecular Physics, Jilin University, Changchun 130023, China.
While planar tetracoordinate (pt) centers have been extensively explored from carbon to other octal-row elements or their heavier analogs, their counterparts involving alkali (A) and alkaline-earth metals (Ae) remain elusive due to the large atomic radius and absence of p orbitals. In this work, we found six hitherto unknown anionic ptA (A4A-) and neutral ptAe (A4Ae) centers through an extensive exploration of potential energy surfaces. The D4h-symmetry ptBe structures in Li4Be and Na4Be emerge as the lowest-energy configurations, and all the other ptA/ptAe structures are higher in energy or saddle points.
View Article and Find Full Text PDFJ Phys Chem A
December 2024
Department of Chemistry, KAIST, Daejeon 34141, Republic of Korea.
The S state relaxation dynamics of chlorobenzene (CB), 3-chlorophenol (3-CP), 3-CP·HO, and 2-chlorophenol·HO (2-CP·HO) have been investigated by means of picosecond time-resolved pump-probe spectroscopy in a state-specific manner. For CB, the S state relaxes via the S-S internal conversion in the low internal energy region (<2000 cm), whereas the direct C-Cl bond dissociation channel mediated by the upper-lying repulsive πσ* state is opened to give the rather sharp increase of the S relaxation rate in the high internal energy region (>2000 cm). A similar dynamic feature has been observed for 3-CP in terms of the lifetime behavior with an increase in the S internal energy, suggesting that the H atom tunneling dissociation reaction from OH might contribute less compared to the internal conversion, although it is not clear at the present time whether or not the sharp increase of the S relaxation rate in the high internal energy region of 3-CP (>1500 cm) is entirely due to that of the internal conversion.
View Article and Find Full Text PDFChem Sci
October 2024
Wydział Chemii, Uniwersytet Wrocławski ul. F. Joliot-Curie 14 50-383 Wrocław Poland
Chemistry
December 2024
Department of Chemistry, Tulane University, New Orleans, LA 70118, USA.
The highly substituted naphthalenes 1,2,3,4,5,6,7-heptaphenylnaphthalene (13), 2,3,4,5,6,7,8-heptaphenyl-1-naphthol (12), 1-bromo-2,3,4,5,6,7,8-heptaphenylnaphthalene (4), and 1-(phenylethynyl)-2,3,4,5,6,7,8-heptaphenylnaphthalene (5) were prepared by a variety of methods, and all but 5 were crystallographically characterized. The attempted Ullmann coupling of 4 to give tetradecaphenyl-1,1'-binaphthyl (3), at both 270 °C and 350 °C, yielded instead 1,2,3,4,5,6-hexaphenylfluoranthene (17) via an intramolecular cyclization reaction. When the alkyne 5 was heated with tetracyclone (6) at 350 °C, 1-(pentaphenylphenyl)-2,3,4,5,6,7,8-heptaphenylnaphthalene (7) was formed in 3 % yield.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
November 2024
Department of Chemistry and Chemical Biology, TU Dortmund University, Otto-Hahn-Strasse 6, 44227, Dortmund, Germany.
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