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| Content Provider | World Health Organization (WHO)-Global Index Medicus |
|---|---|
| Author | Calbo, Joaquín Martín, Nazario Hsieh, Ya-chu Pérez, Emilio M. Pla, Paula Wu, Yao-ting Gallego, María Ortí, Enrique Guldi, Dirk M. Krick Calderon, Rafael M. |
| Description | Author Affiliation: Gallego M ( Departamento de Química Orgánica, Fac. C. C. Químicas, Universidad Complutense de Madrid, Av. Complutense s/n, 28040, Madrid, Spain.); Calbo J ( Instituto de Ciencia Molecular, Universidad de Valencia, 46980, Paterna, Spain.); Krick Calderon RM ( Department of Chemistry and Pharmacy and Interdisciplinary Center for Molecular Materials (ICMM), Friedrich-Alexander-Universität, Erlangen-Nürnberg, 91058, Erlangen, Germany.); Pla P ( Instituto de Ciencia Molecular, Universidad de Valencia, 46980, Paterna, Spain.); Hsieh YC ( Department of Chemistry, National Cheng Kung University, 70101, Tainan, Taiwan.); Pérez EM ( IMDEA Nanociencia, Faraday 9, Campus UAM, 28049, Madrid, Spain.); Wu YT ( Department of Chemistry, National Cheng Kung University, 70101, Tainan, Taiwan.); Ortí E ( Instituto de Ciencia Molecular, Universidad de Valencia, 46980, Paterna, Spain.); Guldi DM ( Department of Chemistry and Pharmacy and Interdisciplinary Center for Molecular Materials (ICMM), Friedrich-Alexander-Universität, Erlangen-Nürnberg, 91058, Erlangen, Germany.); Martín N ( Departamento de Química Orgánica, Fac. C. C. Químicas, Universidad Complutense de Madrid, Av. Complutense s/n, 28040, Madrid, Spain.) |
| Abstract | The association behavior of an electron-donating, bowl-shaped, truxene-based tetrathiafulvalene (truxTTF) with two corannulene-based fullerene fragments, $C_{32}H_{12}$ and $C_{38}H_{14},$ is investigated in several solvents. Formation of 1:1 complexes is followed by absorption titrations and complemented by density functional theory (DFT) calculations. The binding constants are in the range $log K_{a}=2.9–3.5.$ DFT calculations reveal that the most stable arrangement is the conformation in which the 1,3-dithiole ring of truxTTF is placed inside the concave cavity of the corannulene derivative. This arrangement is confirmed experimentally by NMR measurements, and implies that a combination of π–π and CH–π interactions is the driving force for association. Time-dependent DFT calculations reproduce the experimental UV/Vis titrations and provide a detailed understanding of the spectral changes observed. Femtosecond transient absorption studies reveal the processes occurring after photoexcitation of either $C_{32}H_{12}$ or $C_{38}H_{14}$ and their supramolecular associates with truxTTF. In the case of $truxTTF⋅C_{38}H_{14},$ photoexcitation yields the charge-separated state $truxTTF^{.+}⋅C_{38}H_{14}^{.−}$ with a lifetime of approximately 160 ps. |
| ISSN | 09476539 |
| e-ISSN | 15213765 |
| Journal | Chemistry - A European Journal |
| Issue Number | 15 |
| Volume Number | 23 |
| Language | English |
| Publisher | Wiley-VCH;ChemPubSoc Europe |
| Publisher Date | 2017-03-13 |
| Publisher Place | Germany |
| Access Restriction | Open |
| Subject Keyword | Chemistry |
| Content Type | Text |
| Resource Type | Article |
| Subject | Organic Chemistry Catalysis |
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