A meta effect in nonphotochemical processes: the homolytic chemistry of m-methoxyphenol.

J Org Chem

Istituto di Chimica Biomolecolare del CNR, Via del Santuario 110, I-95028 Valverde (CT) Italy.

Published: March 2008

The m-methoxy group is normally electron-withdrawing (EW), sigma(m) = +0.12, sigma(m+) = +0.05. The strong EW activity of a phenoxyl radical's O* atom causes the m-methoxy group to become electron-donating (ED), sigma(m)(+) = -0.14. In valence bond terms, this can be ascribed to the nonclassical resonance structures 1c-e. Although it has long been known that m-methoxy is ED in photoexcited states, it has now been found to be ED for homolytic O-H bond breaking in ground-state 3-methoxyphenol.

Download full-text PDF

Source
http://dx.doi.org/10.1021/jo702520rDOI Listing

Publication Analysis

Top Keywords

m-methoxy group
8
meta nonphotochemical
4
nonphotochemical processes
4
processes homolytic
4
homolytic chemistry
4
chemistry m-methoxyphenol
4
m-methoxyphenol m-methoxy
4
group electron-withdrawing
4
electron-withdrawing sigmam
4
sigmam +012
4

Similar Publications

To study the photophysical and redox properties as a function of -aryl units, a series of hypervalent phosphorus(V) porphyrins, PP(OMe)·PF, PMP(OMe)·PF, PDMP(OMe)·PF, P345TMP(OMe)·PF, and P246TMP(OMe)·PF, with phenyl (P), 4-methoxyphenyl (MP), 3,5-dimethoxyphenyl (DMP), 3,4,5-trimethoxyphenyl (345TMP), and 2,4,6-trimethoxyphenyl (246TMP) units, respectively, have been synthesized. The P(+5) in the cavity makes the porphyrin ring electron-poor, whereas the methoxy groups make the -phenyl rings electron-rich. The presence of electron-rich and electron-poor portions within the porphyrin molecule promoted an intramolecular charge transfer (ICT).

View Article and Find Full Text PDF

Bacterial thiol-disulfide oxidoreductase DsbA is essential for bacterial virulence factor assembly and has been identified as a viable antivirulence target. Herein, we report a structure-based elaboration of a benzofuran hit that bound to the active site groove of Escherichia coli DsbA. Substituted phenyl groups were installed at the 5- and 6-position of the benzofuran using Suzuki-Miyaura coupling.

View Article and Find Full Text PDF

Evaluation of Polar Effects in Hydrogen Atom Transfer Reactions from Activated Phenols.

J Org Chem

February 2019

Dipartimento di Scienze e Tecnologie Chimiche , Università "Tor Vergata", Via della Ricerca Scientifica, 1 I-00133 Rome , Italy.

Evaluation of polar effects in hydrogen atom transfer (HAT) processes is made difficult by the fact that in most cases substrates characterized by lower bond dissociation energies (BDEs), activated from an enthalpic point of view, are also more activated by polar effects. In search of an exception to this general rule, we found that the introduction of a methoxy substituent in the 3-position of 2,6-dimethylphenol results in a small increase in the O-H BDE and a decrease of the ionization potential of the phenol. These findings suggest that the enthalpic effect associated with the addition of the m-methoxy group to 2,6-dimethylphenol will decrease reaction rates, while the polar effects will increase reaction rates.

View Article and Find Full Text PDF

Dimeric cinnamoylamide analogues for regulation of tyrosinase activity in melanoma cells: A role of diamide-link chain length.

Bioorg Med Chem

December 2018

Department of Fine Chemistry, Cosmetic R&D Center, Seoul National University of Science and Technology, 232 Gongneungro, Nowon-gu, Seoul 01811, Republic of Korea. Electronic address:

Dimeric cynnamoyl analogues (DCAs) with depigmenting activity have been developed. In this study, a role of diamide linkage chain length of DCAs as a tyrosinase inhibitor was investigated on tyrosinase inhibitory activity, antioxidative activity, hydrophobicity and anti-melanogenesis as well as structural characteristics and dipole moments based on density functional theory. DCAs with different diamide-link chain lengths (n = 2, 3, and 4) and various functional groups (m-coumaroyl, p-coumaroyl, isoferuloyl and feruloyl groups) were synthesized.

View Article and Find Full Text PDF

m-Methoxy Substituents in a Tetraphenylethylene-Based Hole-Transport Material for Efficient Perovskite Solar Cells.

Chemistry

November 2016

Chongqing Key Laboratory for Advanced Materials, and Technologies of Clean Energy, Faculty of Materials & Energy, Southwest University, Chongqing, 400715, P.R. China.

Three tetrapheynlethylene derivatives (N,N-di(4-methoxyphenyl)aminophenyl-substituted tetraphenylethylene; TPE-4DPA) with different methoxy positions (pp-, pm-, and po-) have been synthesized and characterized. The methoxy groups can control the oxidation potential of the materials, and the electronic properties of the derivatives were affected by the position of the methoxy substituents. These compounds were synthesized in a facile and cost-effective way, and were applied as hole-transport materials in perovskite solar cells.

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!