4.6 Article

Rotationally resolved electronic spectroscopy of 3-cyanoindole and the 3-cyanoindole-water complex

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PHYSICAL CHEMISTRY CHEMICAL PHYSICS
卷 20, 期 36, 页码 23441-23452

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ROYAL SOC CHEMISTRY
DOI: 10.1039/c8cp04020f

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  1. Deutsche Forschungsgemeinschaft [SCHM1043/12-3]
  2. DFG
  3. CONACYT [277871]

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The rotationally resolved electronic spectra of the origin bands of 3-cyanoindole, 3-cyanoindole(d(1)), and the 3-cyanoindole-(H2O)(1) cluster have been measured and analyzed using evolutionary algorithms. For the monomer, permanent dipole moments of 5.90 D for the ground state, and of 5.35 D for the lowest excited singlet state have been obtained from electronic Stark spectroscopy. The orientation of the transition dipole moment is that of an L-1(b) state for the monomer. The water moiety in the water cluster could be determined to be trans-linearly bound to the NH group of 3-cyanoindole, with an NH center dot center dot center dot O hydrogen bond length of 201.9 pm in the electronic ground state. Like the 3-cyanoindole monomer, the 3-cyanoindole-water cluster also shows an L-1(b)-like excited singlet state. The excited state lifetime of isolate 3-cyanoindole in the gas phase has been determined to be 9.8 ns, and that of 3-cyanoindole(d1) has been found to be 14.8 ns, while that of the 1 : 1 water cluster is considerably shorter (3.6 ns). The excited state lifetime of 3-cyanoindole(d(1)) in D2O solution has been found to be smaller than 20 ps.

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