We present a versatile synthesis method capable of creating triphenylene discotic liquids with enhanced control of the number and type of tails. The compounds obtained from this method include a discotic liquid crystal with unusually short methoxy tails.

The synthesis and crystal structures of a series of 6-arylfuvlenes (fulvene is 5-methylidenecyclopenta-1,3-diene) with varying methylation patterns on the 6-phenyl substituent are reported, namely 6-(3-methylphenyl)-1,3-diphenylfulvene (C25H20), 6-(4-methylphenyl)-1,3-diphenylfulvene (C25H20), 6-mesityl-3-diphenylfulvene (C27H24) and 6-(2,3,4,5,6-pentamethylphenyl)-1,3-diphenylfulvene (C29H28). The bond lengths are typical of those observed in related fulvenes. A network of C—H...π ring interactions consolidates the packing in each structure.

Five new crystal structures of perfluoropyridine substituted in the 4-position with phenoxy, 4-bromophenoxy, naphthalen-2-yloxy, 6-bromonaphthalen-2-yloxy, and 4,4′-biphenoxy are reported, viz. 2,3,5,6-tetrafluoro-4-phenoxypyridine, C11H5F4NO (I), 4-(4-bromophenoxy)-2,3,5,6-tetrafluoropyridine, C11H4BrF4NO (II), 2,3,5,6-tetrafluoro-4-[(naphthalen-2-yl)oxy]pyridine, C15H7F4NO (III), 4-[(6-bromonaphthalen-2-yl)oxy]-2,3,5,6-tetrafluoropyridine, C15H6BrF4NO (IV), and 2,2′-bis[(perfluoropyridin-4-yl)oxy]-1,1′-biphenyl, C22H8F8N2O2 (V). The dihedral angles between the aromatic ring systems in I–IV are 78.74 (8), 56.35 (8), 74.30 (7), and 64.34 (19)°, respectively. The complete molecule of V is generated by a crystallographic twofold axis: the dihedral angle between the pyridine ring and adjacent phenyl ring is 80.89 (5)° and the equivalent angle between the biphenyl rings is 27.30 (5)°. In each crystal, the packing is driven by C—H...F interactions, along with a variety of C—F...π, C—H...π, C—Br...N, C—H...N, and C—Br...π contacts. Hirshfeld surface analysis was conducted to aid in the visualization of these various influences on the packing.

Trifluoromethanesulphonylhydroxamic acid, CF3 SO2 NHOH, is shown to release HNO under physiological pH conditions. A two-step synthesis is presented with the first complete characterization of CF3 SO2 NHOH. This molecule rapidly decomposes in neutral aqueous solution to cleanly release HNO and CF3 SO2- , which was demonstrated using the HNO traps TXPTS and HOCbl, and by 19 F NMR spectroscopy.

The title Diels–Alder product, C52H44·2CH3CN, was obtained in trace quantity as the `endo' isomer during the synthesis of 1,3-diphenyl-6-(3,5-dimethylphenyl)fulvene. One of the two co-crystallized acetonitrile molecules is linked to the main molecule by a weak C—H...N hydrogen bond.

Stereoselective syntheses of three new rac di-(tert-butyl)ethano bridged metallocene compounds of Yb, Eu and Sm were carried out by a unique strategy involving hydrocarbon radical anion coupling of a trisubstituted pentafulvene followed by incorporation of the metal by K+ salt metathesis reactions. Reductive coupling of 1,3-diphenyl-6-(tert-butyl) fulvene with sodium naphthalenide gave the corresponding bis(cyclopentadiene) ansa-ligand precursor rac-[(CHBut)(2)(Ph2C5H3)(2)] HL. Subsequent reaction of HL with KN(SiMe3)(2) afforded the corresponding di-potassium salt complex [(CHBut)(2)(Ph2C5H2)(2)]K-2(THF)(3) 1. Reactions of 1 with LnI(2) (Ln = Yb, Eu, Sm) afforded new lanthanide ansa-metallocenes, [(CHBut)(2)(Ph2C5H2)](2)Yb(DME) 2, [(CHBut)(2)(Ph2C5H2)](2)Eu(DME)(2) 3 and [(CHBut)(2)(Ph2C5H2)](2)Sm(DME)(2) 4 in good yields. The ansa-europocene 3 is the first example of a Eu2+ ion complexed by an ethano-bridged cyclopentadienyl ligand. This work underscores the usefulness of hydrocarbon radical anion coupling in the construction of sterically demanding Ph2Cp based ansa-ligand frameworks for d- and f-block metallocenes. Published by Elsevier B.V.

The design, synthesis and photophysical properties of a Low Molecular Weight pH-responsive Gelator (LMWG) based on alkoxy group functionalized DCDHF-Hydrazones (DCDHF-H) are described. A straightforward synthesis of DCDHF-Hydrazone (DCDHF-H) chromophores was achieved via simple azo-coupling starting from 2-(dicyanomethylene)-2,5-dihydro-4,5,5-trimethylfuran-3-carbonitrile and alkoxy bearing aryl diazonium chloride derivatives. The DCDHF-H efficiently gelate selected organic solvents and reversibly respond to pH stimuli with a gel-sol conversion and an associated color change from yellow to purple. Self-assembly of these molecules, as indicated by X-ray crystallography, occurs via cooperative π–π stacking and van der Waals interactions producing gelation in some pure and mixed organic solvents. Furthermore, the presence of acidic or alkaline gases leads to a dramatic change in the rheological properties with potential applications in areas such as gas detection devices and drug release systems. Scanning electron microscopy (SEM) and transmission electron microscopy (TEM) studies of the xerogels obtained from n-propanol provide visual images revealing the formation of fibrous nanostructures.

Multi-stimuli responsive DCDHF-hydrazone molecular switch containing a hydrazone recognition moiety is developed for the naked-eye detection of alkaline analytes in both vapour and aqueous media. Mechanisms accounting for the thermochromism, pH-sensitivity and solvatochromism are proposed. DCDHF-hydrazone chromophores of different substituents introduced nanostructures with different morphologies via a re-precipitation technique. The films formulated from these nanostructures function as solid-state vapochromic sensors for probing alkaline vapours such as amines and ammonia. The sensing performance is reversible and has differential sensitivity towards a variety of amines at comparable concentrations. The structure of the hydrazone molecular switch was established spectroscopically and by single crystal X-ray crystallography.

An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available from the CCDC and typically includes 3D coordinates, cell parameters, space group, experimental conditions and quality measures.

A series of 1,3-diphenyl-6-alkyl/arylfulvenes was prepared, and the electrochemical properties were investigated. The addition of phenyl groups about the fulvene raised the reduction potential and helped to stabilize the electrochemically generated radical anion. The addition of various functional groups onto the phenyl ring at the 6-position of 1,3,6-triphenylfulvene results in a linear free energy relationship between reduction potential and the Hammett substituent constant, σ. Further extending the conjugation at the 6-position of 1,3-diphenyl-6-arylfulvenes increases the reversibility of the redox reactions, but does not appear to further stabilize the generated radical anion. This in-depth investigation provides evidence that the compounds studied may have utility in light-harvesting applications.

The addition of either lithium dimethylamide or lithium diethylamide to a tetrahydrofuran (THF) solution of 1,3-dicyclohexylcarbodiimide yielded THF adducts of lithium 2,2-dimethyl-1,3-dicyclohexylguandidinate (1) and lithium 2,2-diethyl-1,3-dicyclohexylguandidinate (2), respectively. One equivalent of either 1 or 2 was subsequently reacted with one equivalent of Group 11 halide (CuCl, AgBr, and AuCl) to generate oligonuclear complexes with the general formula {M[CyNC(NR2)NCy]}n where M, R, and n are respectively Cu, CH3, 2 (3); Cu, CH2CH3, 2 (4); Ag, CH3, 3 (5); Ag, CH2CH3, 3 (6); Au, CH3, 2 (7); and Au, CH2CH3, 2 (8). Compounds 1–8 were characterized by single-crystal X-ray diffraction. The bulk powders for all complexes were found to be in agreement with the crystal structures based on elemental analyses, Fourier transform infrared spectroscopy, and 1H, 13C, and 7Li NMR studies. The unique structural aspects of this family of Group 11 complexes are highlighted.