Di‐o‐Quinones Bearing an Additional Coordination Function in <i>m</i> ‐Dioxyarylene Linker as Potential Building Blocks for Coordination‐Driven Self‐Assembly

Abstract Bis‐dioxolene ligands 1 – 5 , linked by m ‐dioxyarylene spacers were synthesized. Such ligands are considered as potential building blocks for coordination‐driven design of cage‐like units by self‐assembly mechanism. The peculiarity of new species is in presence of additional functional group in the linker such as pyridinyl ( 1 ), ester ( 2 – 3 ), and carboxyl ( 4 – 5 ) that add the possibilities for ordering modes during the design of coordination polymers. Di‐ o ‐quinones 1–2 were synthesized by reaction of 4‐chloro‐3,6‐di‐ tert ‐butyl‐ o ‐quinone (4‐Cl‐3,6‐Q) with pyridine‐3,5‐diol and methyl 3,5‐dixydroxybenzoate, respectively, in presence of base. The preparation of di‐o‐quinone 5 turned to be a multistage process where di‐catechols 3–4 were isolated as intermediates.

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Journal
ChemistrySelect
Published
2024-11-01
DOI
https://doi.org/10.1002/slct.202403747
Citations
3
Primary Topic
Supramolecular Chemistry and Complexes
Type
article
Field-Weighted Citation Impact
0.75

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article

Di‐o‐Quinones Bearing an Additional Coordination Function in m ‐Dioxyarylene Linker as Potential Building Blocks for Coordination‐Driven Self‐Assembly

V. A. Kuropatov, Н. В. Антипова, V.K. Cherkasov, Anton V. Cherkasov et al.
3 citations
ChemistrySelect
Supramolecular Chemistry and Complexes
0.75
article

Di‐o‐Quinones Bearing an Additional Coordination Function in m ‐Dioxyarylene Linker as Potential Building Blocks for Coordination‐Driven Self‐Assembly

V. A. Kuropatov, Н. В. Антипова, V.K. Cherkasov, Anton V. Cherkasov, Konstantin A. Martyanov, A. V. Cherkasova
article en
3 citations

Abstract

Abstract Bis‐dioxolene ligands 1 – 5 , linked by m ‐dioxyarylene spacers were synthesized. Such ligands are considered as potential building blocks for coordination‐driven design of cage‐like units by self‐assembly mechanism. The peculiarity of new species is in presence of additional functional group in the linker such as pyridinyl ( 1 ), ester ( 2 – 3 ), and carboxyl ( 4 – 5 ) that add the possibilities for ordering modes during the design of coordination polymers. Di‐ o ‐quinones 1–2 were synthesized by reaction of 4‐chloro‐3,6‐di‐ tert ‐butyl‐ o ‐quinone (4‐Cl‐3,6‐Q) with pyridine‐3,5‐diol and methyl 3,5‐dixydroxybenzoate, respectively, in presence of base. The preparation of di‐o‐quinone 5 turned to be a multistage process where di‐catechols 3–4 were isolated as intermediates.

ChemistrySelectVol. 9(42)
G.A. Razuvaev Institute of Organometallic Chemistry (RU)
Russian Science Foundation
Life in Land
Openalex Percentile: Top 31%
Supramolecular Chemistry and Complexes
0.75
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