Electronic polarization spectroscopy of metal phthalocyanine chloride compounds in superfluid helium droplets

被引:11
作者
Pei, Linsen [1 ]
Zhang, Jie [1 ]
Kong, Wei [1 ]
机构
[1] Oregon State Univ, Dept Chem, Corvallis, OR 97331 USA
基金
美国国家科学基金会;
关键词
D O I
10.1063/1.2803186
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We report the electronic polarization spectroscopy of two metal phthalocyanine chloride compounds (MPcCl, M=Al,Ga) embedded in superfluid helium droplets and oriented in a dc electric field. For both compounds, the laser induced fluorescence spectra show preference for perpendicular excitation relative to the orientation field. This result indicates that the permanent dipoles of both compounds are predominantly perpendicular to the transition dipole. Since the permanent dipole derives from the metal chloride, while the transition dipole derives from the phthalocyanine chromophore, in the plane of phthalocyanine, this qualitative result is not surprising. However, quantitative modeling reveals that this intuitive model is inadequate and that the transition dipole might have tilted away from the molecular plane of phthalocyanine. The out of plane component of the transition dipole amounts to similar to 10% if the permanent dipole is assumed to be similar to 4 debye. The origin for this tilt is puzzling, and we tentatively attribute it to the transition of nonbonding orbitals, either from the chlorine atom or from the bridge nitrogen atom, to the pi(*) orbitals of the phthalocyanine chromophore. On the other hand, although unlikely, we cannot completely exclude the possibility that both our high level density functional theory calculation and ab initio results severely deviate from reality. The droplet matrix induces redshifts in the origin of the electronic transition and produces discrete phonon wings. Nevertheless, in dc electric fields, all phonon wings and the zero phonon line demonstrate the same dependence on the polarization direction of the excitation laser. Although electronic excitation does couple to the superfluid helium matrix and the resulting phonon wings add complications to the electronic spectrum, this coupling does not affect the direction of the electronic transition dipole. Electronic polarization spectroscopy in superfluid helium droplets is thus still informative in revealing the permanent dipole and its relation relative to the transition dipole. (c) 2007 American Institute of Physics.
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页数:8
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共 55 条
[1]   Symmetry properties of electronically excited states of nitroaromatic compounds [J].
Abbott, JE ;
Peng, XZ ;
Kong, W .
JOURNAL OF CHEMICAL PHYSICS, 2002, 117 (19) :8670-8675
[2]  
[Anonymous], 1974, TABLES EXPT DIPOLE M
[3]   Molecular control using dc electric fields: Quenching of the tunneling in HF dimer [J].
Bemish, RJ ;
Chan, MC ;
Miller, RE .
CHEMICAL PHYSICS LETTERS, 1996, 251 (3-4) :182-188
[4]   MICROWAVE SPECTRUM, DIPOLE MOMENT, AND NUCLEAR QUADRUPOLE COUPLING CONSTANTS OF PYRIMIDINE [J].
BLACKMAN, GL ;
BROWN, RD ;
BURDEN, FR .
JOURNAL OF MOLECULAR SPECTROSCOPY, 1970, 35 (03) :444-&
[5]   SPECTROSCOPY OF PENDULAR STATES - THE USE OF MOLECULAR-COMPLEXES IN ACHIEVING ORIENTATION [J].
BLOCK, PA ;
BOHAC, EJ ;
MILLER, RE .
PHYSICAL REVIEW LETTERS, 1992, 68 (09) :1303-1306
[6]   SPECTRA OF THE H-2 PHTHALOCYANINE IN LOW-TEMPERATURE MATRICES [J].
BONDYBEY, VE ;
ENGLISH, JH .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1979, 101 (13) :3446-3450
[7]   Helium nanodroplet isolation rovibrational spectroscopy: Methods and recent results [J].
Callegari, C ;
Lehmann, KK ;
Schmied, R ;
Scoles, G .
JOURNAL OF CHEMICAL PHYSICS, 2001, 115 (22) :10090-10110
[8]   Directions of transition dipole moments of t-butyl nitrite obtained via orientation with a strong, uniform electric field [J].
Castle, KJ ;
Kong, W .
JOURNAL OF CHEMICAL PHYSICS, 2000, 112 (23) :10156-10161
[9]   Direction of the transition dipole moment of nitrobenzene determined from oriented molecules in a uniform electric field [J].
Castle, KJ ;
Abbott, J ;
Peng, XH ;
Kong, W .
JOURNAL OF CHEMICAL PHYSICS, 2000, 113 (04) :1415-1419
[10]   Photodissociation of o-nitrotoluene between 220 and 250 nm in a uniform electric field [J].
Castle, KJ ;
Abbott, JE ;
Peng, XZ ;
Kong, W .
JOURNAL OF PHYSICAL CHEMISTRY A, 2000, 104 (45) :10419-10425