{rac-5-[Methoxy(phenyl)methyl]-10,20-diphenylporphyrinato}nickel(II)

The title compound, [Ni(C40H28N4O)], was obtained from a Grignard reaction of the respective formylporphyrin to yield {5-[hydroxy(phenyl)methyl]-10,20-diphenylporphyrinato}nickel(II), followed by crystallization from methylene chloride/methanol. The molecule exhibits a ruffled macrocycle with an ave...

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Main Authors: Mathias O. Senge, Katja Dahms
Format: Article
Language:English
Published: International Union of Crystallography 2011-02-01
Series:Acta Crystallographica Section E
Online Access:http://scripts.iucr.org/cgi-bin/paper?S1600536811002960
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spelling doaj-d630980cbd41461482feb33e52edd6672020-11-24T20:56:10ZengInternational Union of CrystallographyActa Crystallographica Section E1600-53682011-02-01672m265m26510.1107/S1600536811002960{rac-5-[Methoxy(phenyl)methyl]-10,20-diphenylporphyrinato}nickel(II)Mathias O. SengeKatja DahmsThe title compound, [Ni(C40H28N4O)], was obtained from a Grignard reaction of the respective formylporphyrin to yield {5-[hydroxy(phenyl)methyl]-10,20-diphenylporphyrinato}nickel(II), followed by crystallization from methylene chloride/methanol. The molecule exhibits a ruffled macrocycle with an average deviation of the 24 macrocycle atoms from their least-squares plane (Δ24) of 0.26 Å and an average Ni—N bond length of 1.931 (2) Å. In line with the asymmetrical substituent pattern, the degree of distortion is slightly larger at point of attachment of the methoxy(phenyl)methyl residue than at the unsubstituted meso position. The methoxy group attached to the chiral C atom is disordered in a 0.534 (4):0.466 (4) ratio. http://scripts.iucr.org/cgi-bin/paper?S1600536811002960
collection DOAJ
language English
format Article
sources DOAJ
author Mathias O. Senge
Katja Dahms
spellingShingle Mathias O. Senge
Katja Dahms
{rac-5-[Methoxy(phenyl)methyl]-10,20-diphenylporphyrinato}nickel(II)
Acta Crystallographica Section E
author_facet Mathias O. Senge
Katja Dahms
author_sort Mathias O. Senge
title {rac-5-[Methoxy(phenyl)methyl]-10,20-diphenylporphyrinato}nickel(II)
title_short {rac-5-[Methoxy(phenyl)methyl]-10,20-diphenylporphyrinato}nickel(II)
title_full {rac-5-[Methoxy(phenyl)methyl]-10,20-diphenylporphyrinato}nickel(II)
title_fullStr {rac-5-[Methoxy(phenyl)methyl]-10,20-diphenylporphyrinato}nickel(II)
title_full_unstemmed {rac-5-[Methoxy(phenyl)methyl]-10,20-diphenylporphyrinato}nickel(II)
title_sort {rac-5-[methoxy(phenyl)methyl]-10,20-diphenylporphyrinato}nickel(ii)
publisher International Union of Crystallography
series Acta Crystallographica Section E
issn 1600-5368
publishDate 2011-02-01
description The title compound, [Ni(C40H28N4O)], was obtained from a Grignard reaction of the respective formylporphyrin to yield {5-[hydroxy(phenyl)methyl]-10,20-diphenylporphyrinato}nickel(II), followed by crystallization from methylene chloride/methanol. The molecule exhibits a ruffled macrocycle with an average deviation of the 24 macrocycle atoms from their least-squares plane (Δ24) of 0.26 Å and an average Ni—N bond length of 1.931 (2) Å. In line with the asymmetrical substituent pattern, the degree of distortion is slightly larger at point of attachment of the methoxy(phenyl)methyl residue than at the unsubstituted meso position. The methoxy group attached to the chiral C atom is disordered in a 0.534 (4):0.466 (4) ratio.
url http://scripts.iucr.org/cgi-bin/paper?S1600536811002960
work_keys_str_mv AT mathiasosenge rac5methoxyphenylmethyl1020diphenylporphyrinatonickelii
AT katjadahms rac5methoxyphenylmethyl1020diphenylporphyrinatonickelii
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