This work demonstrates that PTA (1,3,5-triaza-7-phosphaadamantane) behaves as an orthogonal ligand between Ru(II) and Zn(II), since it selectively binds through the P atom to ruthenium and through one or more of the N atoms to zinc. This property of PTA was exploited for preparing the two monomeric porphyrin adducts with axially bound PTA, [Ru(TPP)(PTA-κ)] (, TPP = -tetraphenylporphyrin) and [Zn(TPP)(PTA-κ)] (). Next, we prepared a number of heterobimetallic Ru/Zn porphyrin polymeric networks-and two discrete molecular systems-mediated by -bridging PTA in which either both metals reside inside a porphyrin core, or one metal belongs to a porphyrin, either Ru(TPP) or Zn(TPP), and the other to a complex or salt of the complementary metal (i.e., -[RuCl(CO)(PTA-κ)] (), -[RuCl(PTA-κ)] (), Zn(CHCOO), and ZnCl). The molecular compounds , , -[{RuCl(PTA-κ)}{Zn(TPP)}] (), and [{Ru(TPP)(PTA-κ)(PTA-κ)}{ZnCl(OH)}] (), as well as the polymeric species [{Ru(TPP)(PTA-κ)}{Zn(TPP)}] (), -[{RuCl(CO)(PTA-κ)}{Zn(TPP)}] (), -[{RuCl(PTA-κ)}{Zn(TPP)}] (), and [{Ru(TPP)(PTA-κ)}{Zn(CHCOO)(CHOH)(OH)}] (), were structurally characterized by single crystal X-ray diffraction. Compounds , , , and are the first examples of solid-state porphyrin networks mediated by PTA. In , , , , and the bridging PTA has the κ binding mode, whereas in the 2D polymeric layers of it has the triple-bridging mode κ,2. The large number of compounds with the six-coordinate Zn(TPP) (the three polymeric networks of , and , out of five compounds) strongly suggests that the stereoelectronic features of PTA are particularly well-suited for this relatively rare type of coordination. Interestingly, the similar 1D polymeric chains and have different shapes (zigzag in vs "Greek frame" in ) because the {-Ru(PTA-κ)} fragment bridges two Zn(TPP) units with geometry in and with geometry in . Orthogonal "Greek frame" 1D chains make the polymeric network of . Having firmly established the binding preferences of PTA toward Ru(II) and Zn(II), we are confident that in the future a variety of Ru/Zn solid-state networks can be produced by changing the nature of the partners. In particular, there are several inert Ru(II) compounds that feature two or more P-bonded PTA ligands that might be exploited as connectors of well-defined geometry for the rational design of solid-state networks with Zn-porphyrins (or other Zn compounds).
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http://dx.doi.org/10.1021/acs.inorgchem.0c00080 | DOI Listing |
Chemistry
July 2024
Departamento de Química Orgánica, Facultad de Ciencias, Universidad Autónoma de Madrid Cantoblanco, 28049, Madrid, Spain.
Two series of metallo-(Zn(II), Mg(II), and Ru(II)) and free-base phthalocyanines (Pcs) with a carboxyl anchoring group and well-established bulky peripheral substituents (either tert-butyl or bulky 2,6-diisopropylphenoxy) were synthesized and tested as sensitizers in dye-sensitized solar cells (DSSCs). The trend of photovoltaic efficiencies (PCEs) for free-base and metallo Pcs followed the order Zn(II)Pc>Mg(II)Pc≫H2Pc ≈ Ru(II)Pc regardless of the peripheral substitution. Higher efficiencies (4.
View Article and Find Full Text PDFInt J Mol Sci
December 2022
MTA-SZTE Lendület Functional Metal Complexes Research Group, University of Szeged, Dóm tér 7, H-6720 Szeged, Hungary.
Multidrug resistance (MDR) in cancer is one of the major obstacles of chemotherapy. We have recently identified a series of 8-hydroxyquinoline Mannich base derivatives with MDR-selective toxicity, however with limited solubility. In this work, a novel 5-nitro-8-hydroxyquinoline-proline hybrid and its Rh(η5-C5Me5) and Ru(η6-p-cymene) complexes with excellent aqueous solubility were developed, characterized, and tested against sensitive and MDR cells.
View Article and Find Full Text PDFInorg Chem
November 2022
Laboratory of Theoretical and Computational Chemistry, Institute of Theoretical Chemistry, College of Chemistry, Jilin University, Liutiao Road #2, Changchun130061, P. R. China.
The high incidence and difficulties of treatment of cancer have always been a challenge for mankind. Two-photon photodynamic therapy (TP-PDT) as a less invasive technique provides a new perspective for tumor treatment due to its low-energy near-infrared excitation, high targeting, and minor damage. At present, the emerging metal complexes used as the photosensitizers (PSs) in TP-PDT have aroused great interest.
View Article and Find Full Text PDFMolecules
October 2022
Molecular Photonics Group, Van 't Hoff Institute for Molecular Sciences, University of Amsterdam, P.O. Box 94157, 1090 GD Amsterdam, The Netherlands.
Within this work, we review the metal coordination effect on the photophysics of metal dipyrrinato complexes. Dipyrrinato complexes are promising candidates in the search for alternative transition metal photosensitizers for application in photodynamic therapy (PDT). These complexes can be activated by irradiation with light of a specific wavelength, after which, cytotoxic reactive oxygen species (ROS) are generated.
View Article and Find Full Text PDFMolecules
January 2021
Department of Chemistry "Ugo Schiff", Università degli Studi di Firenze, via della Lastruccia 3, 50019 Sesto Fiorentino, Italy.
The synthesis of a new Ru complex, in which the metal is coordinated by two 1,10-phenanthroline ligands and a 2,2'-bipyridyl unit linked, via methylene bridges in its 4 and 4' positions, to two 1,4,7,10-tetraazacyclododecane (cyclen) macrocycles ([Ru(phen) ]) is reported. Protonation and Zn binding by [Ru(phen) ] have been analyzed by potentiometric titration, evidencing the formation of mixed hetero-binuclear and hetero-trinuclear Zn/Ru complexes. These complexes were tested as bis-phenol A (BPA) binders.
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