Repozytorium

AgI/VV heterobimetallic frameworks generated from novel-type {Ag2(VO2F2)2(triazole)4} secondary building blocks: a new aspect in the design of SVOF hybrids.

Autorzy

Ganna A. Senchyk

V. O. Bukhanko

Andrey B. Lysenko

Harald Krautscheid

Eduard B. Rusanov

Alexander N. Chernega

Mirosław Karbowiak

Konstantin V. Domasevitch

Rok wydania

2012

Czasopismo

Inorganic Chemistry

Numer woluminu

51

Strony

8025-8033

DOI

10.1021/ic3000894

Kolekcja

Naukowa

Język

Angielski

Typ publikacji

Artykuł

Streszczenie

A series of new silver(I)-containing MOFs [Ag2(tr2ad)2](ClO4)2 (1), [Ag2(VO2F2)2(tr2ad)2]·H2O (2), [Ag2(VO2F2)2(tr2eth)2(H2O)2] (3), and [Ag2(VO2F2)2(tr2cy)2]·4H2O (4) supported by 4-substituted bifunctional 1,2,4-triazole ligands (tr2ad = 1,3-bis(1,2,4-triazol-4-yl)adamantane, tr2eth = 1,2-bis(1,2,4-triazol-4-yl)ethane, tr2cy = trans-1,4-bis(1,2,4-triazol-4-yl)cyclohexane) were hydrothermally synthesized and structurally characterized. In these complexes, the triazole heterocycle as an N1,N2-bridge links either two adjacent Ag–Ag or Ag–V centers at short distances forming polynuclear clusters. The crystal structure of compound 1 is based on cationic {Ag2(tr)4}2+ fragments connected in a 2D rhombohedral grid network with (4,4) topology. The neighboring layers are tightly packed into a 3D array by means of argentophilic interactions (Ag···Ag 3.28 Å). Bridging between different metal atoms through the triazole groups assists formation of heterobimetallic AgI/VV secondary building blocks in a linear V–Ag–Ag–V sequence that is observed in complexes 24. These unprecedented tetranuclear {Ag2(VO2F2)2(tr)4} units (the intermetal Ag–Ag and Ag–V distances are 4.24–4.36 and 3.74–3.81 Å, respectively), in which vanadium(V) oxofluoride units possess distorted trigonal bipyramidal environment {VO2F2N}¯, are incorporated into 1D ribbon (2) or 2D square nets (3, 4) using bitopic μ4-triazole ligands. The valence bond calculation for vanadium atoms shows +V oxidation state in the corresponding compounds. Thermal stability and photoluminescence properties were studied for all reported coordination polymers.

Adres publiczny

https://doi.org/10.1021/ic3000894

Strona internetowa wydawcy

https://www.acs.org/content/acs/en.html

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