Robust S4 ⋠⋠⋠O Supramolecular Synthons: Structures of Radical-Radical Cocrystals [p-XC6 F4 CNSSN]2 [TEMPO] (X=F, Cl, Br, I, CN).

Cocrystallization of the dithiadiazolyl (DTDA) radicals p-XC6 F4 CNSSN (X=F, Cl, Br, I, CN) with TEMPO afforded the 2 : 1 cocrystals [p-XC6 F4 CNSSN]2 [TEMPO] (1-5) whose structures all reflect a common S4 ⋅⋅⋅O supramolecular motif. The nature of this interaction was probed by DFT calculations (M06/aug-cc-pVDZ) on 1 which revealed that the enthalpy of formation of the [C6 F5 CNSSN]2 [TEMPO] supramolecular motif from [C6 F5 CNSSN]2 and TEMPO is substantial (-54.0 kJ mol-1 ). Electronic structure calculations revealed a TEMPO-based doublet S= 1 / 2 configuration as the ground state with limited spin density on the DTDA rings (2.4 %). The corresponding spin quartet state is +78.9 kJ mol-1 higher in energy. An atoms-in-molecules analysis reveals four bond critical points (BCPs) between the TEMPO O and the DTDA S atoms as well as additional BCPs between selected DTDA S atoms and methyl H atoms of the TEMPO molecule. Herein, the structures of 2-5 are considered within the context of a hierarchical view of competing and complementary intermolecular interactions; in particular, the established supramolecular CN⋅⋅⋅S-S synthon is sacrificed in order to form the new S4 ⋅⋅⋅O interaction.

Inclusion and reactivity of main group radicals in the porous framework MIL-53(Al).

Inclusion of the dithiadiazolyl and diselenadiazolyl radicals PhCNEEN (E = S, Se) into the porous framework, Al(bdc)(OH) [MIL-53(Al); bdc = 1,4-benzenedicarboxylate] was achieved by vacuum sublimation. PXRD studies reveal the inclusion complexes adopt the orthorhombic space group Imma. Variable temperature PXRD studies coupled with thermal analysis reveal that for PhCNSSN@MIL-53(Al), radical elimination from the pores at elevated temperatures is accompanied by an opening of the pore channels. Radicals can also be extracted from the framework using an appropriate solvent. Oxidation of the radical guest within the host framework has been achieved with Cl2 or Br2 and led to complete radical oxidation (based on EPR studies) whereas the milder oxidant I2 leads to incomplete oxidation.

Exploring through-bond and through-space magnetic communication in 1,3,2-dithiazolyl radical complexes.

Reaction of the methyl-benzodithiazolyl radical (MBDTA) with M(hfac)2 complexes (M = Mn, Co, Zn) affords the complexes M(hfac)2(MBDTA)2. Strong antiferromagnetic exchange interactions are observed between M(ii) ions and the two S = 1/2 radicals (M = Mn, Co), whereas weak antiferromagnetic interactions are observed between radicals when using the diamagnetic Zn(ii) ion. Strong intermolecular exchange coupling is also evident in Mn(hfac)2(MBDTA)2 and attributed to π*-π* contacts between MBDTA radicals which are absent for the Co and Zn derivatives.