The BIAN ligand 1,2-bis[(2,6-diisopropylphenyl)imino]acenaphthene: An electron sponge or a „normal“ alpha-diimine ligand?

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388955%3A_____%2F17%3A00467827" target="_blank" >RIV/61388955:_____/17:00467827 - isvavai.cz</a>

Výsledek na webu

<a href="http://dx.doi.org/10.1016/j.ica.2016.05.054" target="_blank" >http://dx.doi.org/10.1016/j.ica.2016.05.054</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1016/j.ica.2016.05.054" target="_blank" >10.1016/j.ica.2016.05.054</a>

Jazyk výsledku

angličtina

Název v původním jazyce

The BIAN ligand 1,2-bis[(2,6-diisopropylphenyl)imino]acenaphthene: An electron sponge or a „normal“ alpha-diimine ligand?

Popis výsledku v původním jazyce

The compounds [fac-Re(CO)(3)C1(L)] and [M(CO)(4)(L)], M = Cr, Mo, W and L = 1,2-bis[(2,6-diisopropylphenyl)imino]acenaphthene, have been studied electrochemically and spectroelectrochemically (IR, UV-vis-NIR, EPR). The neutral rhenium complex contains an isopropyl-shielded chloride ligand. Its reversible oxidation was shown to involve a largely metal-based HOMO. One electron could be added reversibly to the diimine-based LUMO of all complexes, as evident from EPR spectroscopy. However, there was no evidence for the reversible acquisition of more than one electron by L in these complexes, ruling out an electron reservoir functionality with multielectron reactivity. DFT and TD-DFT calculations were performed for the [Re(CO)(3)Cl(L)](n) redox series (n = +, 0, -). (C) 2016 Elsevier B.V. All rights reserved.

Název v anglickém jazyce

The BIAN ligand 1,2-bis[(2,6-diisopropylphenyl)imino]acenaphthene: An electron sponge or a „normal“ alpha-diimine ligand?

Popis výsledku anglicky

The compounds [fac-Re(CO)(3)C1(L)] and [M(CO)(4)(L)], M = Cr, Mo, W and L = 1,2-bis[(2,6-diisopropylphenyl)imino]acenaphthene, have been studied electrochemically and spectroelectrochemically (IR, UV-vis-NIR, EPR). The neutral rhenium complex contains an isopropyl-shielded chloride ligand. Its reversible oxidation was shown to involve a largely metal-based HOMO. One electron could be added reversibly to the diimine-based LUMO of all complexes, as evident from EPR spectroscopy. However, there was no evidence for the reversible acquisition of more than one electron by L in these complexes, ruling out an electron reservoir functionality with multielectron reactivity. DFT and TD-DFT calculations were performed for the [Re(CO)(3)Cl(L)](n) redox series (n = +, 0, -). (C) 2016 Elsevier B.V. All rights reserved.

Druh

J_imp - Článek v periodiku v databázi Web of Science

CEP obor

—

OECD FORD obor

10405 - Electrochemistry (dry cells, batteries, fuel cells, corrosion metals, electrolysis)

Projekt

<a href="/cs/project/LD14129" target="_blank" >LD14129: Struktura a dynamika excitovaných a redoxních stavů fotokatalytických komplexů</a><br>

Návaznosti

I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Rok uplatnění

2017

Kód důvěrnosti údajů

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Název periodika

Inorganica chimica acta

ISSN

0020-1693

e-ISSN

—

Svazek periodika

455

Číslo periodika v rámci svazku

2

Stát vydavatele periodika

NL - Nizozemsko

Počet stran výsledku

9

Strana od-do

540-548

Kód UT WoS článku

000390722500023

EID výsledku v databázi Scopus

2-s2.0-84997106939