Nonplanar porphyrins: synthesis, properties, and unique functionalities

T Ishizuka, N Grover, CJ Kingsbury, H Kotani… - Chemical Society …, 2022 - pubs.rsc.org
Porphyrins are variously substituted tetrapyrrolic macrocycles, with wide-ranging biological
and chemical applications derived from metal chelation in the core and the 18π aromatic …

Porphyrins as molecular electronic components of functional devices

M Jurow, AE Schuckman, JD Batteas… - Coordination chemistry …, 2010 - Elsevier
The proposal that molecules can perform electronic functions in devices such as diodes,
rectifiers, wires and capacitors, or serve as functional materials for electronic or magnetic …

Self-organized porphyrinic materials

CM Drain, A Varotto, I Radivojevic - Chemical reviews, 2009 - ACS Publications
“Anything that exists must be possible.” is often referred to as KE Boulding's First Law. 1 For
example, nanoscale photonic devices exist that harvest light and convert it to …

Conformational control of cofactors in nature–the influence of protein-induced macrocycle distortion on the biological function of tetrapyrroles

MO Senge, SA MacGowan, JM O'Brien - Chemical Communications, 2015 - pubs.rsc.org
Tetrapyrrole-containing proteins are one of the most fundamental classes of enzymes in
nature and it remains an open question to give a chemical rationale for the multitude of …

Modulating the chemical reactivity of gold complexes in living systems: from concept to biomedical applications

J Jiang, X **ong, T Zou - Accounts of Chemical Research, 2023 - ACS Publications
Conspectus Over the past few decades, research on the chemistry of gold has progressed
rapidly, encompassing topics like catalysis, supramolecular chemistry, molecular …

Exercises in molecular gymnastics—bending, stretching and twisting porphyrins

MO Senge - Chemical Communications, 2006 - pubs.rsc.org
The functional versatility of tetrapyrroles as natural cofactors is related to their
conformational flexibility where manipulation of the macrocycle conformation allows a fine …

Naphthyl-Fused π-Elongated Porphyrins for Dye-Sensitized TiO2 Cells

S Hayashi, M Tanaka, H Hayashi, S Eu… - The Journal of …, 2008 - ACS Publications
Novel unsymmetrically π-elongated porphyrins, in which the naphthyl moiety is fused to the
porphyrin core at the naphthyl bridge with a carboxyl group (fused-Zn-1) or at the opposite …

Ultrafast excited state relaxation of a metalloporphyrin revealed by femtosecond X-ray absorption spectroscopy

ML Shelby, PJ Lestrange, NE Jackson… - Journal of the …, 2016 - ACS Publications
Photoexcited Nickel (II) tetramesitylporphyrin (NiTMP), like many open-shell
metalloporphyrins, relaxes rapidly through multiple electronic states following an initial …

meso-Tetra(pentafluorophenyl)porphyrin as an Efficient Platform for Combinatorial Synthesis and the Selection of New Photodynamic Therapeutics using a Cancer …

D Samaroo, M Vinodu, X Chen… - Journal of combinatorial …, 2007 - ACS Publications
The four para fluoro groups on 5, 10, 15, 20-tetrakis-(2, 3, 4, 5, 6-pentafluorophenyl)-
porphyrin (TPPF20) are known to react with a variety of nucleophiles, but the reaction …

Structures and photoinduced electron transfer of protonated complexes of porphyrins and metallophthalocyanines

S Fukuzumi, T Honda, T Kojima - Coordination Chemistry Reviews, 2012 - Elsevier
Porphyrins and phthalocyanines are planar two-dimensional π-compounds, which are
normally difficult to protonate because of the low basicity. When many bulky substituents are …