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Inne
A novel complex of zinc tetraphenylporphyrin with two dioxane molecules in a rare attachment. Crystal structure, spectroscopy and theoretical calculations.
Autorzy
Rok wydania
2013
Czasopismo
Numer woluminu
51
Strony
61-69
DOI
10.1016/j.poly.2012.12.014
Kolekcja
Język
Angielski
Typ publikacji
Artykuł
We have shown the X-ray crystal structure of a novel ZnTPP–(Dioxane)2 complex and the results of solution studies by means of steady state absorption and fluorescence as well as time-resolved fluorescence techniques complemented by theoretical DFT and TD DFT B3LYP/6-31G(d,p) calculations. The ZnTPP–(Dioxane)2 crystallizes in centrosymmetric monoclinic unit cell, space group P21/c and shows a unique structure, with two dioxane molecules in “chair” conformation, placed in equatorial and axial position relative to ZnTPP core. Analysis of TD DFT B3LYP/6-31G(d,p) wave functions of ZnTPP–(Dioxane)2, allowed us to describe the nature of particular electronic transitions and to identify two bands (LE, CT) absent in its components. The former, results from the symmetry reduction of ZnTPP and the latter, from a mixed character of the HOMO (220) orbital of the complex. A red shift of the Soret and the Q band found in absorption and fluorescence spectra indicating the complex formation in solution is confirmed by the simulated absorption spectra of ZnTPP–(Dioxane)2 relative to ZnTPP unit both in the gas phase and in dioxane solution by PCM model. The estimated lifetime of the complex (1.75 ns) is shorter than that of free ZnTPP unit (∼2 ns).
Słowa kluczowe
crystal structure, Complex, dioxane, Zinc tetraphenylporphyrin, exiced states, theoretical calculations
Adres publiczny
http://dx.doi.org/10.1016/j.poly.2012.12.014
Strona internetowa wydawcy
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