Coordination Properties of Porphyrin Analogues Ionized Forms by Experiment and Quantum Chemistry: 5,10,15,20‐Tetraphenyl‐21‐thia‐ and 5,10,15,20‐Tetraphenyl‐21,23‐Dithiaporphyrins-Reference-Cited by-同舟云学术

Coordination Properties of Porphyrin Analogues Ionized Forms by Experiment and Quantum Chemistry: 5,10,15,20‐Tetraphenyl‐21‐thia‐ and 5,10,15,20‐Tetraphenyl‐21,23‐Dithiaporphyrins

Published:2022-12 Issue:45 Volume:7 Page:
ISSN:2365-6549
Container-title:ChemistrySelect
language:en
Short-container-title:ChemistrySelect

Author:

Pukhovskaya Svetlana G.¹,Ivanova Yulia B.²,Syrbu Sergey A.²,Plotnikova Anna O.¹,Kuzmin Ilya A.¹,Pimenov Oleg A.¹,Shlykov Sergey A.¹^ORCID

Affiliation:

1. inorganic chemistry physics and physical and colloidal chemistry Ivanovo State University of Chemistry and Technology Sheremetevskiy ave. 7 153000 Ivanovo Russian Federation

2. New materials based on macrocyclic compounds G.A. Krestov Institute of Solution Chemistry of the Russian Academy of Sciences Academicheskaya st.,1 153045б Ivanovo Russia

Funder

Russian Science Foundation

Publisher

Wiley

Subject

General Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/slct.202202971

Reference76 articles.

1. Metal coordinated pyrrole-based macrocycles as contrast agents for magnetic resonance imaging technologies: Synthesis and applications

2. Porphyrin Conjugates for Cancer Therapy

3. Fe/Mn‐Porphyrin Coordination Polymer Nanoparticles for Magnetic Resonance Imaging (MRI) Guided‐Combination Therapy between Photodynamic Therapy and Chemodynamic Therapy

4. Tetrapyrrolic Macrocycles: Potentialities in Medical Imaging Technologies

5. Amphiphilic meso(sulfonate ester fluoroaryl)porphyrins: refining the substituents of porphyrin derivatives for phototherapy and diagnostics

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