{"id":1093,"date":"2023-06-07T16:07:21","date_gmt":"2023-06-07T14:07:21","guid":{"rendered":"https:\/\/compbat.eu\/?p=1093"},"modified":"2023-06-07T17:29:24","modified_gmt":"2023-06-07T15:29:24","slug":"computational-screening-of-n-alkylated-pyridoxal-derivatives","status":"publish","type":"post","link":"https:\/\/compbat.eu\/2023\/06\/07\/computational-screening-of-n-alkylated-pyridoxal-derivatives\/","title":{"rendered":"Computational screening of N-alkylated pyridoxal derivatives"},"content":{"rendered":"
Computational screening of N-alkylated pyridoxal derivatives is published, here you can find one of our last publications, from the\u00a0Research Centre of Natural Sciences (TTK), the University of Jyv\u00e4skyl\u00e4 and University of Turku teams.<\/p>\n<\/div>\n
Our manuscript entitled \u201cN-alkylated pyridoxal derivatives as negative electrolyte materials for aqueous organic flow batteries: Computational screening\u201d has recently been accepted for publication in the journal Chemistry\u2014A European Journal. The main focus of the contribution is the development and analysis of a molecular database of pyridinium-frameworks.<\/p>\n
The first and highly important step towards elaborating the high-throughput screening of redox active molecules was developing a reliable workflow to generate an initial molecular database. The TTK team established a combined theoretical protocol based on different levels of quantum chemical computations which provides reliable reduction potentials. The protocol was applied to generate the structural and one-electron reduction potential of more than 6700 pyridinium-derivatives included in the B6-PYR molecular library.<\/p>\n
The predicted reduction potentials span a broad range for the investigated pyridinium frameworks. The computational screening revealed that only pyridoxal derivatives give rise to standard reduction potentials compatible with the electrochemical stability window of aqueous electrolytes.<\/p>\n