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TCNQ (7,7,8,8-tetracyanoquinodimethane) anion-radical derivatives were used to fine tune the magnetic properties of the [Co II (Fctp) 2 ] 2+ (Fctp = 4′-(2-ferrocenyl)-2,2′:6′2′′-terpyridine) cation in the solid state. The cocrystallization of [Co II (Fctp) 2 ] 2+ with TCNQ˙ − yielded the two pseudo-polymorphic products [Co II (Fctp) 2 ] (TCNQ) 2 ( 1 ) and [Co II (Fctp) 2 ] (TCNQ) 2 ·MeCN ( 2 ) whereas the analogous reaction with TCNQF˙ − (TCNQF = 2-fluoro-7,7,8,8-tetracyanoquinodimethane) exclusively yielded [Co II (Fctp) 2 ] (TCNQF) 2 ·MeCN ( 3 ). Compound 1 exhibits slow relaxation of magnetization under an applied DC field with U eff = 19.1 K and τ 0 = 9.8 × 10 −6 s. Compounds 2 and 3 are isostructural but exhibit different spin-crossover behavior with transition temperatures of T 1/2 = 336 K and 226 K, respectively. Investigations of the solid state structures by DFT calculations indicate that the differences in magnetic properties of the cationic moiety, [Co II (Fctp) 2 ] 2+ , are induced by supramolecular interactions between [Co II (Fctp) 2 ] 2+ and tunable TCNQ˙ − /TCNQF˙ − anion-radical derivatives.
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Regioselective [2 + 2] cycloaddition reaction within a pair of polymorphic co-crystals based upon halogen bonding interactions
The realization of a pair of photoreactive polymorphic co-crystals that are held together by the combination of I⋯N halogen bonding interactions and C–H⋯Cl contacts is reported. The reactant molecule within these co-crystals is based upon an unsymmetrical olefin, namely 4-stilbazole, that results in a regioselective solid-state [2 + 2] cycloaddition reaction in both polymorphic forms. Each solid undergoes a quantitative photoreaction which yields exclusively the head-to-tail photoproduct.
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- Award ID(s):
- 1827756
- PAR ID:
- 10157973
- Date Published:
- Journal Name:
- CrystEngComm
- Volume:
- 21
- Issue:
- 43
- ISSN:
- 1466-8033
- Page Range / eLocation ID:
- 6671 to 6675
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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- Free Publicly Accessible Full Text
-
Accepted Manuscript1.0
- Journal Article:
- https://doi.org/10.1039/c9ce01379b
