Back to Search Start Over

Subcomponent self-assembly of circular helical Dy 6 (L) 6 and bipyramid Dy 12 (L) 8 architectures directed via second-order template effects.

Authors :
Li XL
Zhao L
Wu J
Shi W
Struch N
Lützen A
Powell AK
Cheng P
Tang J
Source :
Chemical science [Chem Sci] 2022 Jul 22; Vol. 13 (34), pp. 10048-10056. Date of Electronic Publication: 2022 Jul 22 (Print Publication: 2022).
Publication Year :
2022

Abstract

In situ metal-templated (hydrazone) condensation also called subcomponent self-assembly of 4,6-dihydrazino-pyrimidine, o -vanillin and dysprosium ions resulted in the formation of discrete hexa- or dodecanuclear metallosupramolecular Dy <subscript>6</subscript> (L) <subscript>6</subscript> or Dy <subscript>12</subscript> (L) <subscript>8</subscript> aggregates resulting from second-order template effects of the base and the lanthanide counterions used in these processes. XRD analysis revealed unique circular helical or tetragonal bipyramid architectures in which the bis(hydrazone) ligand L adopts different conformations and shows remarkable differences in its mode of metal coordination. While a molecule of trimethylamine acts as a secondary template that fills the void of the Dy <subscript>6</subscript> (L) <subscript>6</subscript> assembly, sodium ions take on this role for the formation of heterobimetallic Dy <subscript>12</subscript> (L) <subscript>8</subscript> by occupying vacant coordination sites, thus demonstrating that these processes can be steered in different directions upon subtle changes of reaction conditions. Furthermore, Dy <subscript>6</subscript> (L) <subscript>6</subscript> shows an interesting spin-relaxation energy barrier of 435 K, which is amongst the largest values within multinuclear lanthanide single-molecular magnets.<br />Competing Interests: The authors declare no conflict of interest.<br /> (This journal is © The Royal Society of Chemistry.)

Details

Language :
English
ISSN :
2041-6520
Volume :
13
Issue :
34
Database :
MEDLINE
Journal :
Chemical science
Publication Type :
Academic Journal
Accession number :
36128245
Full Text :
https://doi.org/10.1039/d2sc03156f