The Redox Activity of Two Identical Units on Xylylene-Bridged N‑Pyridinium-Substituted Diamino-1,3,5-triazine
Abstract
The N-benzylpyridinium-substituted diamino-1,3,5-triazine (Bz-TZN) and its geometrically separated units on a xylene core (O-, M-, P-TZN) were synthesized. The cyclic voltammetry of these compounds shows two redox states, irrespective of the number and location on the xylene core. These compounds were characterized by 1H, 13C NMR, HRMS, CV, chronoamperometry, staircase voltammetry, and spectroelectrochemistry, which revealed that two units on a xylene core have negligible interaction with each other and mostly retain their independent redox states.
Read the paper
Related studies
- eggNOG 5.0: a hierarchical, functionally and phylogenetically annotated orthology resource based on 5090 organisms and 2502 viruses
- Online Survival Analysis Software to Assess the Prognostic Value of Biomarkers Using Transcriptomic Data in Non-Small-Cell Lung Cancer
- OptiType: precision HLA typing from next-generation sequencing data
- Nicotinic Cholinergic System and COVID-19: In Silico Identification of an Interaction between SARS-CoV-2 and Nicotinic Receptors with Potential Therapeutic Targeting Implications
- Saccharomyces cerevisiae cells have three Omega class glutathione S-transferases acting as 1-Cys thiol transferases
- Hemolysis at low blood flow rates: in-vitro and in-silico evaluation of a centrifugal blood pump
Go deeper in Evidence Hub
Evidence Hub adds a study data sheet (design, sample size, evidence level, key numbers), an AI summary and a chat grounded in the paper's text.