期刊
PHYSICAL CHEMISTRY CHEMICAL PHYSICS
卷 14, 期 37, 页码 12905-12911出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c2cp41636k
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资金
- Spanish MICINN (Juan de la Cierva) [FIS2010-65702-C02-01, PIB2010US-00652, /CSD2010-00044/]
- Grupos Consolidados UPV/EHU del Gobierno Vasco [IT-319-07]
- European Research Council Advanced Grant DYNamo (ERC-AdG [267374]
- European Research Council Advanced Grant DYNamo (SGIker ARINA UPV/EHU)
- Lundbeckfonden
- FNU
Charge-transfer excitations highly depend on the electronic coupling between the donor and acceptor groups. Nitrophenolates are simple examples of charge-transfer systems where the degree of coupling differs between ortho, meta and para isomers. Here we report the absorption spectra of the isolated anions in vacuo to avoid the complications of solvent effects. Gas-phase action spectroscopy was done with two different setups, an electrostatic ion storage ring and an accelerator mass spectrometer. The results are interpreted on the basis of CC2 quantum chemical calculations. We identified absorption maxima at 393, 532, and 399 nm for the para, meta, and ortho isomer, respectively, with the charge-transfer transition into the lowest excited singlet state. In the meta isomer, this pi-pi* transition is strongly redshifted and its oscillator strength reduced, which is related to the pronounced charge-transfer character, as a consequence of the topology of the conjugated pi-system. Each isomer's different charge distribution in the ground state leads to a very different solvent shift, which in acetonitrile is bathochromic for the para and ortho, but hypsochromic for the meta isomer.
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