Hallmarks of anticancer and antimicrobial activities of corroles

VK Sharma, YG Assaraf, Z Gross - Drug Resistance Updates, 2023 - Elsevier
Corroles provide a remarkable opportunity for the development of cancer theranostic agents
among other porphyrinoids. While most transition metal corrole complexes are only …

Recent advances in the functionalization of formyl and acroleyl appended corroles

I Yadav, D Dhiman, M Sankar - Chemical Communications, 2024 - pubs.rsc.org
The field of corrole systems particularly those with functional groups at their peripheral
positions has experienced a surge of interest in recent years, driven by their exceptional …

Molecular structures and absorption spectra assignment of corrole NH tautomers

W Beenken, M Presselt, TH Ngo… - The Journal of …, 2014 - ACS Publications
The individual absorption spectra of the two NH tautomers of 10-(4, 6-dichloropyrimidin-5-yl)-
5, 15-dimesitylcorrole are assigned on the basis of the Gouterman four-orbital model and a …

Строение и оптические свойства тетрапиррольных соединений

НН Крук - 2019 - elib.belstu.by
Монография обобщает современные представления о строении, молекулярной
конформации, электронной структуре, спектрально-люминесцентных характеристиках …

Photophysical properties of β-substituted free-base corroles

CM Lemon, RL Halbach, M Huynh… - Inorganic …, 2015 - ACS Publications
Corroles are an emergent class of fluorophores that are finding an application and reaction
chemistry to rival their porphyrin analogues. Despite a growing interest in the synthesis …

Molecular structure and conformation of free base corroles

M Wouter - Макрогетероциклы, 2019 - cyberleninka.ru
Corroles represent a unique family of tetrapyrrolic chromophores with distinct structural,
chemical and photophysical properties, which render them promising materials for …

Free-Base Corrole Anion

A Tarai, J Mallick, P Singh, J Conradie… - The Journal of …, 2023 - ACS Publications
Free-base corroles have long been known to be acidic, readily undergoing deprotonation by
mild bases and in polar solvents. The conjugate base, however, has not been structurally …

Fluorenyl-corroles: Characterization, photophysical, photobiological, and DNA/BSA-binding properties of novel examples

BM Rodrigues, CC Diniz, MH Köhler… - … of Photochemistry and …, 2025 - Elsevier
In this study, it was evaluated the photophysical, electrochemical, photobiological, and
DNA/BSA-binding properties of fluorenyl corrole derivatives H 3 MFluCor and H 3 TFluCor …

Effects of Substituents on the Photophysical/Photobiological Properties of Mono-Substituted Corroles

VB de Souza, VN da Rocha, PC Piquini, OA Chaves… - Molecules, 2023 - mdpi.com
The trans-A2B-corrole series was prepared starting with 5-(pentafluorophenyl)
dipyrromethene, which was then reacted with respective aryl-substituted aldehyde by Gryko …

NH Tautomerism of N-confused porphyrin: Solvent/substituent effects and isomerization mechanism

T Ishizuka, R Sakashita, O Iwanaga… - The Journal of …, 2020 - ACS Publications
The effects of substituents and solvents on the NH tautomerism of N-confused porphyrin (2)
were investigated. The structures, electronic states, and aromaticity of NH tautomers (2-2H …