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超流氦滴中氯代金属酞菁化合物的电极化光谱

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

作者信息

Pei Linsen, Zhang Jie, Kong Wei

机构信息

Department of Chemistry, Oregon State University, Corvallis, Oregon 97331-4003, USA.

出版信息

J Chem Phys. 2007 Nov 7;127(17):174308. doi: 10.1063/1.2803186.

Abstract

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 approximately 10% if the permanent dipole is assumed to be approximately 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.

摘要

我们报告了嵌入超流氦滴中并在直流电场中取向的两种金属酞菁氯化物化合物(MPcCl,M = Al,Ga)的电子极化光谱。对于这两种化合物,激光诱导荧光光谱显示相对于取向场更倾向于垂直激发。该结果表明这两种化合物的永久偶极子主要垂直于跃迁偶极子。由于永久偶极子源自金属氯化物,而跃迁偶极子源自酞菁发色团,在酞菁平面内,这个定性结果并不令人惊讶。然而,定量建模表明这个直观模型并不充分,并且跃迁偶极子可能已经偏离了酞菁的分子平面。如果假设永久偶极子约为4德拜,则跃迁偶极子的平面外分量约为10%。这种倾斜的起源令人费解,我们初步将其归因于非键轨道从氯原子或桥连氮原子到酞菁发色团的π*轨道的跃迁。另一方面,虽然不太可能,但我们不能完全排除我们的高水平密度泛函理论计算和从头算结果都严重偏离实际的可能性。液滴基质在电子跃迁的原点处引起红移并产生离散的声子边带。然而,在直流电场中,所有声子边带和零声子线对激发激光的偏振方向表现出相同的依赖性。尽管电子激发确实与超流氦基质耦合,并且产生的声子边带给电子光谱增加了复杂性,但这种耦合并不影响电子跃迁偶极子的方向。因此,超流氦滴中的电子极化光谱在揭示永久偶极子及其与跃迁偶极子的关系方面仍然具有参考价值。

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