Crystal structures of three platinacyclic complexes bearing isopropyl eugenoxyacetate and pyridine derivatives

Three new platinum(II) complexes bearing a eugenol and a pyridine derivative, namely (η2-2-allyl-4-methoxy-5-{[(propan-2-yloxy)carbonyl]methoxy}phenyl-κC1)chlorido(pyridine-κN)platinum(II), [Pt(C15H19O4)Cl(C5H5N)], (I), (η2-2-allyl-4-methoxy-5-{[(propan-2-yloxy)carbonyl]methoxy}phenyl-κC1)chlorido(4...

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Main Authors: Nguyen Thi Thanh Chi, Pham Van Thong, Luc Van Meervelt
Format: Article
Language:English
Published: International Union of Crystallography 2020-07-01
Series:Acta Crystallographica Section E: Crystallographic Communications
Subjects:
Online Access:http://scripts.iucr.org/cgi-bin/paper?S2056989020006957
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spelling doaj-bf80d30197424106b42f2aa1b466026b2020-11-25T03:03:17ZengInternational Union of CrystallographyActa Crystallographica Section E: Crystallographic Communications2056-98902020-07-017671012101710.1107/S2056989020006957mw2159Crystal structures of three platinacyclic complexes bearing isopropyl eugenoxyacetate and pyridine derivativesNguyen Thi Thanh Chi0Pham Van Thong1Luc Van Meervelt2Department of Chemistry, Hanoi National University of Education, 136 Xuan Thuy, Cau Giay, Hanoi, VietnamDepartment of Chemistry, Hanoi National University of Education, 136 Xuan Thuy, Cau Giay, Hanoi, VietnamDepartment of Chemistry, KU Leuven, Biomolecular Architecture, Celestijnenlaan 200F, Leuven (Heverlee), B-3001, BelgiumThree new platinum(II) complexes bearing a eugenol and a pyridine derivative, namely (η2-2-allyl-4-methoxy-5-{[(propan-2-yloxy)carbonyl]methoxy}phenyl-κC1)chlorido(pyridine-κN)platinum(II), [Pt(C15H19O4)Cl(C5H5N)], (I), (η2-2-allyl-4-methoxy-5-{[(propan-2-yloxy)carbonyl]methoxy}phenyl-κC1)chlorido(4-methylpyridine-κN)platinum(II), [Pt(C15H19O4)Cl(C6H7N)], (II), and (η2-2-allyl-4-methoxy-5-{[(propan-2-yloxy)carbonyl]methoxy}phenyl-κC1)chlorido(pyridine-4-carboxylic acid-κN)platinum(II), [Pt(C15H19O4)Cl(C6H5NO2)], (III), have been synthesized and further characterized by single-crystal X-ray diffraction. The PtII atoms exhibit the usual distorted square-planar coordination and are surrounded by one Cl atom, one N atom, and a C atom and C=C double bond of the eugenol ligand. The donor N atom of the pyridine ligand occupies a cis position with respect to the double bond. Complexes (I) and (II) crystallize isomorphously in space group P\overline{1} and display a similar crystal packing characterized by C—H...O hydrogen bonding, C—H...π and π–π interactions. However, the presence of the additional methyl group in the 4-methylpyridine ligand in (II) disturbs the π–π interactions. The crystal packing of (III) is characterized by O—H...O hydrogen bonding, resulting in the formation of chains of molecules connected in a head-to-tail fashion and running in the [101] direction. The IC50 values for the HepG2 and KB cell lines are 150.9, 122.3 µM for (I) and 138.9, 93.2 µM for (II), respectively.http://scripts.iucr.org/cgi-bin/paper?S2056989020006957crystal structureplatinum(ii) complexeseugenolpyridine derivativescytotoxicity
collection DOAJ
language English
format Article
sources DOAJ
author Nguyen Thi Thanh Chi
Pham Van Thong
Luc Van Meervelt
spellingShingle Nguyen Thi Thanh Chi
Pham Van Thong
Luc Van Meervelt
Crystal structures of three platinacyclic complexes bearing isopropyl eugenoxyacetate and pyridine derivatives
Acta Crystallographica Section E: Crystallographic Communications
crystal structure
platinum(ii) complexes
eugenol
pyridine derivatives
cytotoxicity
author_facet Nguyen Thi Thanh Chi
Pham Van Thong
Luc Van Meervelt
author_sort Nguyen Thi Thanh Chi
title Crystal structures of three platinacyclic complexes bearing isopropyl eugenoxyacetate and pyridine derivatives
title_short Crystal structures of three platinacyclic complexes bearing isopropyl eugenoxyacetate and pyridine derivatives
title_full Crystal structures of three platinacyclic complexes bearing isopropyl eugenoxyacetate and pyridine derivatives
title_fullStr Crystal structures of three platinacyclic complexes bearing isopropyl eugenoxyacetate and pyridine derivatives
title_full_unstemmed Crystal structures of three platinacyclic complexes bearing isopropyl eugenoxyacetate and pyridine derivatives
title_sort crystal structures of three platinacyclic complexes bearing isopropyl eugenoxyacetate and pyridine derivatives
publisher International Union of Crystallography
series Acta Crystallographica Section E: Crystallographic Communications
issn 2056-9890
publishDate 2020-07-01
description Three new platinum(II) complexes bearing a eugenol and a pyridine derivative, namely (η2-2-allyl-4-methoxy-5-{[(propan-2-yloxy)carbonyl]methoxy}phenyl-κC1)chlorido(pyridine-κN)platinum(II), [Pt(C15H19O4)Cl(C5H5N)], (I), (η2-2-allyl-4-methoxy-5-{[(propan-2-yloxy)carbonyl]methoxy}phenyl-κC1)chlorido(4-methylpyridine-κN)platinum(II), [Pt(C15H19O4)Cl(C6H7N)], (II), and (η2-2-allyl-4-methoxy-5-{[(propan-2-yloxy)carbonyl]methoxy}phenyl-κC1)chlorido(pyridine-4-carboxylic acid-κN)platinum(II), [Pt(C15H19O4)Cl(C6H5NO2)], (III), have been synthesized and further characterized by single-crystal X-ray diffraction. The PtII atoms exhibit the usual distorted square-planar coordination and are surrounded by one Cl atom, one N atom, and a C atom and C=C double bond of the eugenol ligand. The donor N atom of the pyridine ligand occupies a cis position with respect to the double bond. Complexes (I) and (II) crystallize isomorphously in space group P\overline{1} and display a similar crystal packing characterized by C—H...O hydrogen bonding, C—H...π and π–π interactions. However, the presence of the additional methyl group in the 4-methylpyridine ligand in (II) disturbs the π–π interactions. The crystal packing of (III) is characterized by O—H...O hydrogen bonding, resulting in the formation of chains of molecules connected in a head-to-tail fashion and running in the [101] direction. The IC50 values for the HepG2 and KB cell lines are 150.9, 122.3 µM for (I) and 138.9, 93.2 µM for (II), respectively.
topic crystal structure
platinum(ii) complexes
eugenol
pyridine derivatives
cytotoxicity
url http://scripts.iucr.org/cgi-bin/paper?S2056989020006957
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