Saddle-shaped tetraphenylenes with peripheral gallic esters displaying columnar mesophases

• Eugen Wuckert,
• Constanze Hägele,
• Frank Giesselmann,
• Angelika Baro and
• Sabine Laschat

Beilstein J. Org. Chem. 2009, 5, No. 57, doi:10.3762/bjoc.5.57

• purification the desired gallic ester-substituted tetraphenylenes 2a–l in 19–72%. In some cases purification turned out to be rather tedious resulting in decreased yields. Mesomorphic properties of compounds 2 were studied by differential scanning calorimetry (DSC), polarizing optical microscopy (POM) and X

• patterns recorded with an imaging plate detector (Fuji BAS SR). In the flat-film camera, the sample was placed in a small hole of a brass block, the temperature of which was controlled by a Lakeshore controller and kept in a 1.5 T magnetic field for alignment. Differential scanning calorimetry (DSC) was

Novel banana-discotic hybrid architectures

• Hari Krishna Bisoyi,
• H. T. Srinivasa and
• Sandeep Kumar

Beilstein J. Org. Chem. 2009, 5, No. 52, doi:10.3762/bjoc.5.52

• discotic dimers. The chemical structures have been characterized by spectral techniques and elemental analysis. The thermal behaviors of the compounds have been investigated by polarizing optical microscopy and differential scanning calorimetry. None of these synthesized compounds exhibit any liquid

• behavior of the novel compounds have been observed by polarizing optical microscopy and differential scanning calorimetry. All the solvent crystallized compounds pass from crystalline state to isotropic liquid state on heating, and on cooling they crystallize into the solid state without any intervening

• differential scanning calorimetry measurements. The absence of either B-phase or discotic columnar mesophase in compound 6 may be explained as follows: since the five-ring banana unit, which otherwise exhibits mesophase with two terminal alkyl chains, is now attached with two bulky triphenylene units at the

A convenient method for preparing rigid-core ionic liquid crystals

• Julien Fouchet,
• Laurent Douce,
• Benoît Heinrich,
• Richard Welter and
• Alain Louati

Beilstein J. Org. Chem. 2009, 5, No. 51, doi:10.3762/bjoc.5.51

• , differential scanning calorimetry and X-ray diffraction. In addition its lamellar crystal structure, electrochemical behaviour and UV (absorption and emission) properties are reported. Keywords: imidazolium; ionic liquid crystals; Ullman reaction; Introduction Over the past decade extensive studies of ionic

• general stability order to be I−< BF4− ≈ PF6−< CF3SO3−< (CF3SO2)2N− (Figure 4). For all the compounds, the mesomorphic behaviour and phase transition temperatures were investigated by polarized optical microscopy (POM), differential scanning calorimetry (DSC), and powder X-ray diffractometry (XRD). To

• were studied with a Leitz polarizing microscope equipped with a Mettler FP80 hot stage and an FP80 central processor. The TGA measurements were carried out on a SDTQ 600 apparatus at scanning rate of 10 °C·min−1. The transition temperatures and enthalpies were measured by differential scanning

Synthesis of mesogenic phthalocyanine-C₆₀ donor–acceptor dyads designed for molecular heterojunction photovoltaic devices

• Yves Henri Geerts,
• Olivier Debever,
• Claire Amato and
• Sergey Sergeyev

Beilstein J. Org. Chem. 2009, 5, No. 49, doi:10.3762/bjoc.5.49

• ) mesophases. Upon heating, transitions to isotropic liquid were observed at 120 °C and 90 °C for 2c and 2d, respectively. For 2c this transition was only detectable by POM and not by differential scanning calorimetry (DSC), while for 2d DSC on heating revealed an endothermic peak at 90 °C [enthalpy 2.7 kJ/mol

Pd/C- Mediated synthesis of indoles in water

• Mohosin Layek,
• Udaya Lakshmi,
• Dipak Kalita,
• Deepak K. Barange,
• Aminul Islam,
• K. Mukkanti and
• Manojit Pal

Beilstein J. Org. Chem. 2009, 5, No. 46, doi:10.3762/bjoc.5.46

• ) are given in hertz. Infrared spectra were recorded on a FTIR spectrometer. Melting points were determined by using thermal analysis and differential scanning calorimetry (DSC) was generated with the help of DSC-60A dector. MS spectra were obtained on a mass spectrometer. Chromatographic (HPLC) purity