A series of parasubstituted tetraphenylporphyrin zirconium(IV) salicylate complexes (SA/5-SSAZr(IV)RTPP, R = p-H, p-CH3, p-NO2, p-Cl, SA = salicylate, and 5-SSA = 5-sulfosalicylate) have been synthesized, and the spectral properties of free base porphyrins, their corresponding metallated, and axially ligated zirconium(IV) porphyrin compounds were compared with each other. A detailed analysis of ultraviolet-visible (UV-vis), proton nulcear magnetic resonance ((1)H NMR) spectroscopy, infrared (IR) spectroscopy, and elemental analysis suggested the transformation from free base porphyrins to zirconium(IV) porphyrins. The ability of the metal in this complex for extra coordination of solvent molecules was confirmed by ESI-MS spectra. Besides the fluorescence, cyclic voltammetry, and thermogravimetric studies, the complexes were also screened for antimicrobial and anticancer activities. Among all the complexes, 5-SSAZr(p-NO2TPP) shows high antibacterial activity.
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http://dx.doi.org/10.1155/2013/903616 | DOI Listing |
European J Org Chem
January 2021
Chiral zirconium(IV) double cage sandwich complex has been synthesized in one step from porphyrin cage was obtained as a racemate, which was resolved by HPLC and the enantiomers were isolated in >99.5 % ee. Their absolute configurations were assigned on the basis of X-ray crystallography and circular dichroism spectroscopy.
View Article and Find Full Text PDFAnal Chem
April 2017
Nagoya Institute of Technology , Graduate School of Engineering, Gokiso, Showa, Nagoya, Japan , 466-8555.
Ion-selective electrode using zirconium(IV) complex with octaethylporphin (Hoep) as a carrier showed high selectivity to triphosphate (TP, Htp) against other hydrophilic anions including diphosphate and phosphate. The electroactive species was identified to be [(Zr(oep)(Htp)] (TP/Zr ratio of 0.5) of the unique structure; triphosphates are recognized by one Zr atom through three O atoms on three different P atoms and by another Zr atom through two O atoms on two terminal P atoms and are also involved in complementary intermolecular hydrogen bonding to be surrounded by four porphyrin complexes.
View Article and Find Full Text PDFACS Nano
December 2015
Department of Chemistry, Northwestern University, 2145 Sheridan Road, Evanston, Illinois 60208, United States.
The nanocrystals of a porphyrin-based zirconium(IV) metal-organic framework (MOF) are used as a dual-function catalyst for the simultaneous detoxification of two chemical warfare agent simulants at room temperature. Simulants of nerve agent (such as GD, VX) and mustard gas, dimethyl 4-nitrophenyl phosphate and 2-chloroethyl ethyl sulfide, have been hydrolyzed and oxidized, respectively, to nontoxic products via a pair of pathways catalyzed by the same MOF. Phosphotriesterase-like activity of the Zr6-containing node combined with photoactivity of the porphyrin linker gives rise to a versatile MOF catalyst.
View Article and Find Full Text PDFBioinorg Chem Appl
October 2013
P.G. Department of Chemistry, University of Jammu, Jammu, Jammu and Kashmir 180006, India.
A series of parasubstituted tetraphenylporphyrin zirconium(IV) salicylate complexes (SA/5-SSAZr(IV)RTPP, R = p-H, p-CH3, p-NO2, p-Cl, SA = salicylate, and 5-SSA = 5-sulfosalicylate) have been synthesized, and the spectral properties of free base porphyrins, their corresponding metallated, and axially ligated zirconium(IV) porphyrin compounds were compared with each other. A detailed analysis of ultraviolet-visible (UV-vis), proton nulcear magnetic resonance ((1)H NMR) spectroscopy, infrared (IR) spectroscopy, and elemental analysis suggested the transformation from free base porphyrins to zirconium(IV) porphyrins. The ability of the metal in this complex for extra coordination of solvent molecules was confirmed by ESI-MS spectra.
View Article and Find Full Text PDFChem Commun (Camb)
November 2012
Department of Chemistry, University of California, Berkeley, California, 94720, USA.
The lithium corrole complex (Mes(2)(p-OMePh)corrole)Li(3)·6THF (1·6THF), prepared via deprotonation of the free-base corrole with lithium amide, acts as precursor for the preparation of cyclopentadienyl zirconium(iv) corrole (2) and pentamethylcyclopentadienyl titanium(IV) corrole (3).
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