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The β-phase of the radical p-NCC6F4CNSSN (1β) crystallizes in the orthorhombic space group Fdd2 and orders as a canted antiferromagnet with TN = 36 K. Computational studies (B3LYP or M06-2X functional with the cc-pVTZ-PP(-F)+basis set) of the microscopic nearest-neighbour magnetic exchange coupling in 1β and in the hypothetical isomorphous phase of the selenium radical p-NCC6F4CNSeSeN (2β) revealed that replacement of S by Se should lead to a significant enhancement in the magnetic ordering temperature by ca. 20% (B3LYP) – 30% (M06-2X). Recrystallization of 2 from solution or via vacuum sublimation afforded only the known diamagnetic, dimeric phase, 2α. Computational studies indicated that both the molecular geometry and charge distribution for 1 and 2 are extremely similar and experimental approaches to form alloys of the general form 11−x2x were explored: attempts to cosublime 1 and 2in vacuo were unsuccessful, forming only 1β due to the low volatility of 2. Crystallization of pure 1 by solution evaporation was found to afford polymorph 1α (triclinic, P1¯) selectively, irrespective of the solvent employed (CH2Cl2, MeCN, PhMe or THF) but 1α transformed to 1β upon subsequent vacuum sublimation. Crystallization of 1 in the presence of 2 (up to 20 mol%) from solution evaporation was examined. At 20 mol% there was clear evidence for formation of both 1α and 2α as distinct crystallographic phases by powder X-ray diffraction (PXRD) but some evidence for doping of 2 into 1α at low concentration (≤15 mol percent) was observed. Attempts to sublime a sample of 10.920.1 led to phase separation with the isolation of needle-shaped crystals of pure 1β characterized by X-ray diffraction. [ABSTRACT FROM AUTHOR]

Mechanochemical synthesis provides new pathways for the rational design of multi-component crystals (MCCs) involving anionic or cationic components that offer molecular-level architectures unavailable to MCCs comprising strictly neutral components. Structural characterization of the products of mechanochemical syntheses is essential for divining clear relationships between the nature of coformers, milling conditions, reaction mechanisms, and intermolecular bonding. Notably, when powder X-ray diffraction and solid-state NMR (SSNMR) are combined with plane-wave density functional theory (DFT) calculations, they offer opportunities for NMR crystallographic solutions and structural refinements. Herein, we report mechanochemical syntheses of five urea-containing MCCs of the form NR4Cl:xUrea·yH2O (R = H, Et, n-Pr; x = 1, 2, 3; y = 0, 2), which can be made in high yields (> ca. 99%) and great rapidity (<40 minutes). We demonstrate the utility of 35Cl SSNMR for providing distinct fingerprints for each urea MCC and detecting chlorine-containing impurities. Dispersion-corrected plane-wave DFT-D2* calculations are used for structural refinement and relating 35Cl electric field gradient (EFG) tensors and chloride ion hydrogen bonding environments. Finally, ab initio molecular dynamics calculations are used to study the impact of molecular motions on 35Cl EFG tensors, and their concomitant use for site assignment and NMR crystallography. Together, these techniques show great promise for future development of crystal structure prediction protocols using NMR of quadrupolar nuclei. [ABSTRACT FROM AUTHOR]

Cocrystallization of the dithiadiazolyl (DTDA) radicals p‐XC6F4CNSSN (X=F, Cl, Br, I, CN) with TEMPO afforded the 2 : 1 cocrystals [p‐XC6F4CNSSN]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 [C6F5CNSSN]2[TEMPO] supramolecular motif from [C6F5CNSSN]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. [ABSTRACT FROM AUTHOR]

The synthesis and reactivity patterns of the strained dithiete ring are compared with their dimeric tetrathiocin counterparts and higher oligomers, highlighting: (i) their cycloaddition chemistry with organic dienophiles as a route to sulfur-containing heterocycles; (ii) their oxidative addition chemistry to low valent transition metal complexes to generate transition metal dithiolate complexes and; (iii) the base-catalysed isomerizations between different dithiete oligomers. [ABSTRACT FROM AUTHOR]

The β-phase of the radical p -NCC 6 F 4 CNSSN (1β) crystallizes in the orthorhombic space group F d d 2 and orders as a canted antiferromagnet with T N = 36 K. Computational studies (B3LYP or M06-2X functional with the cc-pVTZ-PP(-F)+basis set) of the microscopic nearest-neighbour magnetic exchange coupling in 1β and in the hypothetical isomorphous phase of the selenium radical p -NCC 6 F 4 CNSeSeN (2β) revealed that replacement of S by Se should lead to a significant enhancement in the magnetic ordering temperature by ca. 20% (B3LYP) - 30% (M06-2X). Recrystallization of 2 from solution or via vacuum sublimation afforded only the known diamagnetic, dimeric phase, 2α. Computational studies indicated that both the molecular geometry and charge distribution for 1 and 2 are extremely similar and experimental approaches to form alloys of the general form 1 1- x 2 x were explored: attempts to cosublime 1 and 2 in vacuo were unsuccessful, forming only 1β due to the low volatility of 2. Crystallization of pure 1 by solution evaporation was found to afford polymorph 1α (triclinic, P 1̄) selectively, irrespective of the solvent employed (CH 2 Cl 2 , MeCN, PhMe or THF) but 1α transformed to 1β upon subsequent vacuum sublimation. Crystallization of 1 in the presence of 2 (up to 20 mol%) from solution evaporation was examined. At 20 mol% there was clear evidence for formation of both 1α and 2α as distinct crystallographic phases by powder X-ray diffraction (PXRD) but some evidence for doping of 2 into 1α at low concentration (≤15 mol percent) was observed. Attempts to sublime a sample of 1 0.9 2 0.1 led to phase separation with the isolation of needle-shaped crystals of pure 1β characterized by X-ray diffraction.

A tridentate ligand LH3 ((2-hydroxy-3-methoxybenzylidene)-2-(hydroxyimino)propanehydrazide) comprising o -vanillin, hydrazone and oxime donor groups has been employed to prepare a series of tetranuclear Ln(III) complexes. The reaction of ligand LH3 with Ln(NO 3 ) 3 [Ln = Sm, Eu, Gd, Tb, Dy, Ho, Er] in MeOH yielded Ln 4 ( LH ) 6 (MeOH) 2 (Ln = Sm(1), Eu(2), Gd(3), Tb(4), Ho (6) and Er (7))] whereas the corresponding reaction with Dy(NO 3 ) 3 afforded Dy 4 ( LH ) 4 ( LH 2 ) 2 (OH) 2 (5). All complexes were characterized by various analytical techniques including single crystal X-ray diffraction, IR spectroscopy, UV-Vis spectroscopy, and elemental analysis. To investigate the potential of these lanthanide complexes for wound healing applications, their effects on fibroblast viability, migration, and M2 macrophage polarization were evaluated. The cytotoxicity assessment revealed that complexes 2(Eu), 4(Tb), 5(Dy), and 7(Er) significantly enhanced fibroblast viability compared to the negative control (NC). In vitro wound healing assay demonstrated that complexes 2(Eu) and 7(Eu) substantially promoted fibroblast migration compared to the NC. Moreover, complex 2(Eu) exhibited significant anti-inflammatory effects by reducing the phagocytic ability of lipopolysaccharide (LPS)-stimulated macrophage cells and attenuating nitric oxide (NO) production. In conclusion, among the series of complexes tested, complex 2(Eu) displayed the most potent anti-inflammatory effect on macrophage cells, while simultaneously promoting fibroblast viability and migration. This unique combination of properties renders complex 2 (Eu) highly promising for wound healing applications.

An efficient and mild reaction protocol for the decarbonylation of isocyanates has been developed using catalytic amounts of Lewis acidic boranes. The electronic nature (electron withdrawing, electron neutral, and electron donating) and the position of the substituents (ortho/meta/para) bound to isocyanate controls the chain length and composition of the products formed in the reaction. Detailed DFT studies were undertaken to account for the formation of the mono/di-carboxamidation products and benzoxazolone compounds., (© 2022 The Authors. Chemistry - A European Journal published by Wiley-VCH GmbH.)

Cocrystallization of the dithiadiazolyl (DTDA) radicals p-XC 6 F 4 CNSSN (X=F, Cl, Br, I, CN) with TEMPO afforded the 2 : 1 cocrystals [p-XC 6 F 4 CNSSN] 2 [TEMPO] (1-5) whose structures all reflect a common S 4 ⋅⋅⋅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 [C 6 F 5 CNSSN] 2 [TEMPO] supramolecular motif from [C 6 F 5 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 S 4 ⋅⋅⋅O interaction., (© 2022 Wiley-VCH GmbH.)

A family of substituted 1,2,4-benzothiadiazine 1-chlorides have been prepared by treatment of N -arylamidines in neat thionyl chloride at reflux. The S(iv) 1-chlorides are readily reduced under mild conditions to persistent 1,2,4-benzothiadiazinyl radicals which have been characterised by EPR spectroscopy and cyclic voltammetry. Crystallographic studies on isolated radicals indicate that the radicals dimerise via pancake bonding in the solid-state, resulting in spin-pairing and net diamagnetism., Competing Interests: There are no conflicts to declare., (This journal is © The Royal Society of Chemistry.)

The synthesis and reactivity patterns of the strained dithiete ring are compared with their dimeric tetrathiocin counterparts and higher oligomers, highlighting: (i) their cycloaddition chemistry with organic dienophiles as a route to sulfur-containing heterocycles; (ii) their oxidative addition chemistry to low valent transition metal complexes to generate transition metal dithiolate complexes and; (iii) the base-catalysed isomerizations between different dithiete oligomers.