Slow Magnetic Relaxation in a Californium Complex.

We report the synthesis and characterization of the macrocyclic californium derivative Na[Cf(HO)(DOTA)] (DOTA = 1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetate), , which was studied in comparison to its dysprosium counterpart, Na[Dy(HO)(DOTA)], . Divergent spectroscopic and magnetic behaviors were observed between and . Based upon spectroscopic measurements, we propose that accessible 5f → 6d transitions (potentially operating in tandem with charge-transfer transitions) are the major contributors to the observed broadband photoluminescence in .

High-Spin Blatter's Triradicals.

Robust organic triradicals with high-spin quartet ground states provide promising applications in molecular magnets, spintronics, In this context, a triradical based on Blatter's radical has been synthesized recently, having two low-lying non-degenerate doublet states with a quartet ground state. The traditional broken-symmetry (BS)-DFT computed doublet-quartet energy gaps are reported to be somewhat overestimated in comparison to the experimentally observed values. In this work, we have employed different methods on this prototypical system to obtain more accurate doublet-quartet energy gaps for this triradical.

A study of [2 + 2] cycloaddition-retroelectrocyclization in water: observation of substrate-driven transient-nanoreactor-induced new reactivity.

Organic solvents limit [2 + 2] cycloaddition-retroelectrocyclization (CA-RE) in biological fields. We examined the formation of 1,1,4,4-tetracyanobuta-1,3-dienes (TCBDs) through CA-RE reactions and their unusual reactivity to produce N-heterocyclic compounds when the nature of the surfactant and the concentrations were varied in the aqueous phase. An environment in which transient self-assemblies (vesicles) were induced by the substrate and surfactant molecules initiated new reactivity through HO addition on the TCBD, generating the enol form of the intermediate, which results in the formation of the 6,6-dicyano-heteropentafulvene (amidofulvene) compound, while lamellar sheets at higher concentrations favored TCBD generation.

Anti-ohmic nanoconductors: myth, reality and promise.

The recent accomplishment in the design of molecular nanowires characterized by increasing conductance with length has led to the origin of an extraordinary new family of molecular junctions referred to as "anti-ohmic" wires. Herein, this highly desirable, non-classical behavior, has been examined for molecules long-enough to exhibit pronounced diradical character in their ground state within the unrestricted DFT formalism with spin symmetry breaking. We demonstrate that highly conjugated acenes signal higher resistance in an open-shell singlet (OSS) configuration as compared to their closed-shell counterparts.

Tuning the magnetic properties of a diamagnetic di-Blatter's zwitterion to antiferro- and ferromagnetically coupled diradicals.

In the quest of obtaining organic molecular magnets based on stable diradicals, we have tuned the inherent zwitterionic ground state of tetraphenylhexaazaanthracene (TPHA), a molecule containing two Blatter's moieties, by adopting two different strategies. In the first strategy, we have increased the length of the coupler between the two radical moieties and observed a transition from the zwitterionic ground state to the diradicalized state. With a larger coupler, ferromagnetic interactions are realized based on density functional theory (DFT) and wave-function theory (WFT) based complete active space self-consistent field (CASSCF)-N-electron valence state perturbation theory (NEVPT2) methods.

Auxiliary Atomic Relay Center Facilitates Enhanced Magnetic Couplings in Blatter's Radical.

The recent accomplishments in obtaining strong ferromagnetic exchange interactions in organic diradicals have made the field quite fascinating and even more promising toward its technological applications. In this context, herein, we report a unique combination of remarkably strong ferromagnetic exchange interactions coupled with molecular rigidity, utilizing superstable Blatter's radical as a spin source. The planar analogues of the parent Blatter's radical obtained by annulation with a chalcogen coupled to nitronyl nitroxide (NN) are investigated using density functional theory along with the wave function-based multiconfigurational self-consistent field methods, for example, complete active space self-consistent field (CASSCF)-N-electron valence state perturbation theory (NEVPT2).

How Plausible Is Getting Ferromagnetic Interactions by Coupling Blatter's Radical via Its Fused Benzene Ring?

With ongoing efforts to synthesize super-stable Blatter's diradicals having strong ferromagnetic exchange interactions, all the 10 possible isomers of di-Blatter diradical coupled through the fused benzene rings are investigated. A variety of electronic structure theory such as broken-symmetry methods in density functional theory (DFT), spin-constraint DFT (CDFT), and wave function-based multi-configurational methods, e.g.

Designing of Push-Pull Chromophores with Tunable Electronic and Luminescent Properties Using Urea as the Electron Donor.

Urea-functionalized 4-ethynylbenzenes undergo facile formal [2 + 2] cycloaddition followed by retroelectrocyclization upon reaction with tetracyanoethylene, yielding 1,1,4,4-tetracyanobuta-1,3-dienes-based push-pull chromophores. Unlike the ,'-dialkylamino group, urea functionalization provides easy access to further functionalization on these chromophores. The resulting chromophores exhibit unexpected white light emissions apart from various inherent properties like intramolecular charge-transfer band and redox behavior.

Iodo-Functionalized Salicylideneimine-Boron Complexes: Synthesis and Photosensitized Degradation of Organic Water Pollutants.

Boron-containing organic compounds are reported to have excellent luminescent properties, however, their ability to photosensitize singlet oxygen generation remains unexplored. The synthesis of several Schiff-base based boranils is reported, starting from commercially available salicylaldehydes and anilines. The iodo-functionalized derivatives were observed to aid in the photosensitized generation of singlet oxygen.