Molecular And Solid‐State Structure Of Oxovanadium(IV) Etioporphyrin‐III

Author:

Pakhomov Georgy L.12,Koptyaev Andrey I.12,Yunin Pavel A.13,Somov Nikolay V.3,Semeikin Alexander S.2,Rychikhina Ekaterina D.2ORCID,Stuzhin Pavel A.2

Affiliation:

1. Institute for Physics of Microstructures of the Russian Academy of Sciences (IPM RAS) GSP-105 Nizhny Novgorod 603950 Russian Federation

2. Ivanovo State University of Chemistry and Technology (ISUCT) 7 Sheremetievskiy Ave Ivanovo 153000 Russian Federation

3. Lobachevsky State University of Nizhny Novgorod (UNN) 23 Gagarin ave Nizhny Novgorod 603022 Russian Federation

Abstract

AbstractOxovanadium(IV) etioporphyrin‐III, VO‐EtioP‐III is an important member of the petroporphyrin family. It can be isolated from crude oil or synthesized de novo from the dipyrromethene precursors, the latter being the approach we used in our research. The molecular structure of VO‐EtioP‐III was for the first time characterized by single‐crystal X‐ray diffraction. Both terminal alkyls and the axial oxygen atom protrude in the same direction relative to the molecular plane, while rear side of the molecule remains almost flat. This results in a peculiar centrosymmetric packing (space group P21/c, monoclinic system with four molecules per unit cell), in which back‐to‐back oriented molecules form the parallel‐plane dimers. The powder X‐ray diffraction data indicate that the VO‐EtioP‐III films deposited by vacuum evaporation retain a very strong texture, with all molecules standing vertically on the substrate surface. The absorption spectra of films differ from the solution spectra by a large redshift of the Soret‐ and Q‐ band (~30 nm) with hypo‐ and hyperchromic effects, respectively. The former band strongly broadens due to multiple splitting to within 350–520 nm, which is followed by a change of the color from purple (in diluted solutions) to brawn (in films or crystals).

Publisher

Wiley

Subject

General Chemistry

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