First entry into nonmetal-centred porphycenes: synthesis of a phosphorus(v) complex of octaethylporphycene.

Dalton Trans

Graduate School of Material Science, University of Hyogo, 3-2-1 Koto, Kamigori-cho, Ako-gun, Hyogo 678-1297, Japan.

Published: February 2018

AI Article Synopsis

Article Abstract

A phosphorus(v) complex of porphycene [P(OEPc)(OMe)]PF (OEPc = 2,3,6,7,12,13,16,17-octaethylporphycenato dianion) has been synthesized and structurally characterized as the first porphycene derivative incorporating nonmetal elements in the macrocyclic cavity. An extremely low energy level of the LUMO is observed, which is rationalized by the low-lying π* orbital of the porphycene ring coupled with the insertion of the highly-inductive pentavalent phosphorus centre. The compound is luminescent in bright red with a quantum yield of 22.7% in CHCl at 298 K.

Download full-text PDF

Source
http://dx.doi.org/10.1039/c7dt04471bDOI Listing

Publication Analysis

Top Keywords

phosphorusv complex
8
entry nonmetal-centred
4
nonmetal-centred porphycenes
4
porphycenes synthesis
4
synthesis phosphorusv
4
complex octaethylporphycene
4
octaethylporphycene phosphorusv
4
complex porphycene
4
porphycene [poepcome]pf
4
[poepcome]pf oepc
4

Similar Publications

We report the extension of the common β-diketimine proligand class, nacnacH (HC(RCNAr)H), where R is an alkyl group such as Et or iPr, plus Ph, and Ar is a sterically demanding aryl substituent such as Dip = 2,6-diispropylphenyl, Dep = 2,6-diethylphenyl, Mes = 2,4,6-trimethylphenyl or mesityl, Xyl = 2,6-dimethylphenyl, one-pot condensation procedures. When a condensation reaction is carried out using the chemical dehydrating agent PPSE (polyphosphoric acid trimethylsilylester), β-diketiminate phosphorus(V) products such as (nacnac)PO can also be obtained, which can be converted to the respective proligand nacnacH alkaline hydrolysis. The nacnacH proligands can be converted to their alkali metal complexes with common methods and we have found that deprotonation of nacnacH is significantly more sluggish than that of related β-diketimines with smaller backbone alkyl groups.

View Article and Find Full Text PDF

Protein Photodamaging Activity and Photocytotoxic Effect of an Axial-Connecting Phosphorus(V)porphyrin Trimer.

Chem Res Toxicol

September 2023

HAMAMATSU BioPhotonics Innovation Chair, Preeminent Medical Photonics Education & Research Center, Hamamatsu University School of Medicine, Handayama 1-20-1, Higashi-ku, Hamamatsu 431-3192, Japan.

An axial-connecting trimer of the porphyrin phosphorus(V) complex was synthesized to evaluate the relaxation process of the photoexcited state and the photosensitizer activity. The photoexcitation energy was localized on the central unit of the phosphorus(V)porphyrin trimer. The photoexcited state of the central unit was relaxed through a process similar to that of the monomer phosphorus(V)porphyrin.

View Article and Find Full Text PDF

Photodynamic antitumor activity of Gallium(III) and Phosphorus(V) complexes of trimethoxyl AB triaryl corrole.

Bioorg Chem

December 2022

School of Chemistry and Chemical Engineering, Key Laboratory of Functional Molecular Engineering of Guangdong Province, South China University of Technology, Guangzhou 510641, China. Electronic address:

Two new trimethoxyl AB triaryl corroles 10-(2,4,6-trimethoxyphenyl)-5,15-bis(pentafluorophenyl)- corrole (1) and 10-(3,4,5-trimethoxyphenyl)-5,15-bis(pentafluorophenyl)-corrole (2) and their gallium(III) and phosphorus(V) (1-Ga, 1-P, 2-Ga and 2-P) complexes had been prepared and well characterized by UV-vis, NMR and HR-MS. Among all compounds, 2-Ga, 1-P and 2-P showed excellent in vivo photodynamic activity against the MDA-MB-231, A549, Hela and HepG2 cell lines upon light irradiation at 625 nm. And 2-P even exhibited higher phototoxicity than the clinical photosensitizer temoporfin.

View Article and Find Full Text PDF

Access to Enantiomerically Pure P-Stereogenic Primary Aminophosphine Sulfides under Reductive Conditions.

Chemistry

December 2022

Institut für Anorganische Chemie, Fakultät für Chemie und Pharmazie, Universität Regensburg, Universitätsstraße 31, 93053, Regensburg, Germany.

Stereochemically pure phosphines with phosphorus-heteroatom bonds and P-centered chirality are a promising class of functional building blocks for the design of chiral ligands and organocatalysts. A route to enantiomerically pure primary aminophosphine sulfides was opened through stereospecific reductive C-N bond cleavage of phosphorus(V) precursors by lithium in liquid ammonia. The chemoselectivity of the reaction as a function of reaction time, substrate pattern, and chiral auxiliary was investigated.

View Article and Find Full Text PDF

Non-Metallic Phosphorus Corrole as Efficient Electrocatalyst in Hydrogen Evolution Reaction.

ChemSusChem

November 2022

Department of Chemistry, Guangdong Provincial Key Laboratory of Fuel Cell Technology & School of Chemistry and Chemical Engineering, South China University of Technology, 510640, Guangzhou, P. R. China.

The economical consideration of using an electrocatalyst in energy-related field, composed of non-precious/sustainable elements is quite noteworthy. In this work, the phosphorus(V) complex of tris-(pentafluorophenyl)corrole [(TPFC)P (OH) ] was reported as electrocatalyst for the hydrogen evolution reaction (HER). The electrochemical studies revealed that the HER experienced a ECEC pathway (E: electron transfer step, C: chemical step), and the possible intermediate [P ]-H species was suggested.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!