Unknown

Dataset Information

0

Dimethylnonacethrene - en route to a magnetic switch.


ABSTRACT: Dimethylnonacethrene is the first derivative of the cethrene family that is energetically more stable than the product of its electrocyclic ring closure. Compared to the shorter homologue dimethylcethrene, the new system is EPR-active, because of a significantly lowered singlet-triplet gap, and displays remarkable stability. Our results suggest that adjustment of the steric bulk in the fjord region can enable realisation of diradicaloid-based magnetic photoswitches.

SUBMITTER: Cavlovic D 

PROVIDER: S-EPMC10281489 | biostudies-literature | 2023 Jun

REPOSITORIES: biostudies-literature

altmetric image

Publications

Dimethylnonacethrene - <i>en route</i> to a magnetic switch.

Čavlović Daniel D   Blacque Olivier O   Krummenacher Ivo I   Braunschweig Holger H   Ravat Prince P   Juríček Michal M  

Chemical communications (Cambridge, England) 20230620 50


Dimethylnonacethrene is the first derivative of the cethrene family that is energetically more stable than the product of its electrocyclic ring closure. Compared to the shorter homologue dimethylcethrene, the new system is EPR-active, because of a significantly lowered singlet-triplet gap, and displays remarkable stability. Our results suggest that adjustment of the steric bulk in the fjord region can enable realisation of diradicaloid-based magnetic photoswitches. ...[more]

Similar Datasets

| S-EPMC31852 | biostudies-literature
| S-EPMC4438431 | biostudies-literature
| S-EPMC4470469 | biostudies-literature
| S-EPMC4360783 | biostudies-literature
| S-EPMC7497115 | biostudies-literature
| S-EPMC3282722 | biostudies-literature
| S-EPMC7969005 | biostudies-literature
| S-EPMC7561000 | biostudies-literature
| S-EPMC10086060 | biostudies-literature
| S-EPMC2956469 | biostudies-literature