Chemical Properties and Facts of 56413-95-7

The article 《Structural factors influencing the intramolecular charge transfer and photoinduced electron transfer in tetrapyrazinoporphyrazines》 also mentions many details about this compound(56413-95-7)Category: chiral-oxygen-ligands, you can pay attention to it or contacet with the author([email protected]) to get more information.

Novakova, Veronika; Hladik, Petr; Filandrova, Tereza; Zajicova, Ivana; Krepsova, Veronika; Miletin, Miroslav; Lenco, Juraj; Zimcik, Petr published the article 《Structural factors influencing the intramolecular charge transfer and photoinduced electron transfer in tetrapyrazinoporphyrazines》. Keywords: tetrapyrazinoporphyrazine synthesis intramol charge transfer photoinduced electron structural factor; magnesium complex tetrapyrazinoporphyrazine synthesis absorption fluorescence quantum yield; zinc complex tetrapyrazinoporphyrazine synthesis absorption fluorescence quantum yield.They researched the compound: 5,6-Dichloropyrazine-2,3-dicarbonitrile( cas:56413-95-7 ).Category: chiral-oxygen-ligands. Aromatic heterocyclic compounds can be divided into two categories: single heterocyclic and fused heterocyclic. In addition, there is a lot of other information about this compound (cas:56413-95-7) here.

Unsym. tetrapyrazinoporphyrazines (TPyzPzs) from the group of azaphthalocyanines with one peripherally attached amino substituent (donor) were synthesized, and their photophys. properties (fluorescence quantum yield and singlet oxygen quantum yield) were determined The synthesized TPyzPzs were expected to undergo intramol. charge transfer (ICT) as the main pathway for deactivating their excited states. Several structural factors play a critical role in ICT efficiency. The substituent in the ortho position to the donor center significantly influences the ICT, with tert-butylsulfanyl and butoxy substituents inducing the strongest ICTs, whereas chloro, Me, Ph, and hydrogen substituents in this position reduce the efficiency. The strength of the donor pos. influences the ICT efficiency and correlates well with the oxidation potential of the amines used as the substituents on the TPyzPz as follows: n-butylamine < N,N-diethylamine < aniline < phenothiazine. The ICT (with conjugated donors and acceptors) in the TPyzPz also proved to be much stronger than a photoinduced electron transfer in which the donor and the acceptor are connected through an aliphatic linker. The article 《Structural factors influencing the intramolecular charge transfer and photoinduced electron transfer in tetrapyrazinoporphyrazines》 also mentions many details about this compound(56413-95-7)Category: chiral-oxygen-ligands, you can pay attention to it or contacet with the author([email protected]) to get more information.

Reference:
Synthesis and Crystal Structure of a Chiral C3-Symmetric Oxygen Tripodal Ligand and Its Applications to Asymmetric Catalysis,
Chiral lanthanide(III) complexes of sulphur–nitrogen–oxygen ligand derived from aminothiourea and sodium D-camphor-β-sulfonate