A study on natural coral stone—a fractal solid

This present research work contains the study of natural fractal material, coral stone. X-ray diffraction, FTIR, optical, DC and AC electrical characteristics are studied. The study includes Arrhenius like plots for both wafer and powder form of the material. Measurements show a possible partially irreversible phase transition occurs when coral is heated for a long time at an about 115?°C. From the XRD data it has been also established that coral stone contains nano sized clusters which is supported by DC electrical measurement. The variation of AC conductivity of coral with thickness of the sample is studied and found exhibit an interesting feature of fractal solid. A scaling relation between AC conductivity and thickness has also been proposed here. The overall behavior of the specimen is like that of a fractal system.     

Effect of acceptor heteroatoms on π-hydrogen bonding interactions: A study of indole⋅⋅⋅thiophene heterodimer in a supersonic jet

Resonant two photon ionization (R2PI), IR-UV, and UV-UV double resonance spectroscopic techniques combined with quantum chemistry calculations have been used to determine the structure of indole???thiophene dimer observed in a supersonic jet. With the help of combined experimental and theoretical IR spectra it has been found that the observed dimer has a N-H???π hydrogen bonded slanted T-shaped structure. The present study demonstrates the effect of heteroatoms present in the acceptors on the strength of the π-hydrogen bonding interactions. It was concluded by Sherrill and co-workers from their theoretical study of benzene???pyridine dimer that aromatic rings containing heteroatoms are poorest π-hydrogen bond acceptors [E. G. Hohenstein and C. D. Sherrill, J. Phys. Chem. A 113, 878 (2009)]. But the current spectroscopic investigation exhibits that five membered aromatic heterocycles are favorable π-hydrogen bond acceptors. In this study, it has also been shown that thiophene is a better π-hydrogen bond acceptor than furan. The present work has immense biological significance as indole is the chromophore of tryptophan residue in the proteins and thiophene derivatives have potential therapeutic applications. Thus, understanding the binding motif between indole and thiophene in the heterodimer studied in this work may help in designing efficient drugs.     

Coordination induced fluorescence enhancement and construction of a Zn3 constellation through hydrolysis of ligand imine arms

The phenoxido and alkoxido bridged neutral Zn(3) complex [Zn(3)(μ-H(2)bemp)(2)(μ(3)-emp)(2)] (1), with an angular Zn(3)(μ-OPh)(2)(μ-OEt)(2) core and capping nitrogen donors, was synthesized via simultaneous chelation-cum-bridging of the parent and hydrolysed ligands. Zinc(II) coordination triggered the solution phase imine (C=N) bond hydrolysis of H(3)bemp (2,6-bis-[(2-hydroxyethylimino)methyl]-4-methylphenol) and yielded the unexpected angular trinuclear Zn(II) complex 1, having structural similarity with the Zn(3) active site of P1 nuclease. H(3)bemp also displays a zinc(II) selective chelation-enhanced fluorescence response from strong metal ion coordination. Complexation of zinc(II) with H(3)bpmp (2,6-bis-[(3-hydroxypropylimino)methyl]-4-methylphenol), a close analogue of H(3)bemp, instead provides only mononuclear [Zn(H(2)bpmpH(N))(2)](ClO(4))(2)·2H(2)O (2·2H(2)O) (H(N) is the proton attached to an imine nitrogen atom) of two zwitterionic ligands, generated through a kind of coordination driven acid-base reaction, without showing any aggregation reaction. As the sole metal-organic precursor, both the complexes under pyrolytic conditions give ZnO nano structures of two morphologies.     

Structure of 7-azaindole···2-fluoropyridine dimer in a supersonic jet: competition between N-H···N and N-H···F interactions

In the present work, we have investigated the structure of 7-azaindole···2-fluoropyridine dimer in a supersonic jet by employing resonant two photon ionization (R2PI), IR-UV, and UV-UV double resonance spectroscopic techniques combined with quantum chemistry calculations. The R2PI spectrum of the dimer is recorded by electronic excitation of the 7-azaindole moiety, and a few low frequency intermolecular vibrations of the dimer are clearly observed in the spectrum. The electronic origin band of the dimer is red-shifted by 1278 cm(-1) from the S(1) ← S(0) origin band of 7-azaindole monomer. The presence of a single conformer of the dimer is confirmed by IR-UV and UV-UV hole-burning spectroscopic techniques. RIDIR (Resonant ion dip infrared) spectrum of the dimer shows a red-shift of 265 cm(-1) in the N-H stretching frequency with respect to that of the 7-azaindole monomer. Two planar double hydrogen bonded cyclic structures of the dimer have been predicted from DFT calculations. Comparison of experimental and theoretical N-H stretching frequencies confirms that the observed dimer is stabilized by N-H···N and C-H···N hydrogen bonding interactions. The less stable conformer with N-H···F and C-H···N interactions are not observed in the experiment. The competition between N-H···N and N-H···F interactions in the two dimeric structures are discussed from natural bond orbital (NBO) analysis. The current results demonstrate that fluorine makes a hydrogen bond of intermediate strength through cooperative interaction of another hydrogen bond (C-H···N) present in the dimer, although fluorine is believed to be very weak hydrogen bond acceptor.     

Hybrid opto-electric manipulation in microfluidics-opportunities and challenges

Hybrid opto-electric manipulation in microfluidics/nanofluidics refers to a set of methodologies employing optical modulation of electrokinetic schemes to achieve particle or fluid manipulation at the micro- and nano-scale. Over the last decade, a set of methodologies, which differ in their modulation strategy and/or the length scale of operation, have emerged. These techniques offer new opportunities with their dynamic nature, and their ability for parallel operation has created novel applications and devices. Hybrid opto-electric techniques have been utilized to manipulate objects ranging in diversity from millimetre-sized droplets to nano-particles. This review article discusses the underlying principles, applications and future perspectives of various hybrid opto-electric techniques that have emerged over the last decade under a unified umbrella.     

A Sandwich Azobenzene–Diamide Dimer for Photoregulated Chloride Transport

There has been a tremendous evolution for artificial ion transport systems, especially gated synthetic systems, which closely mimic their natural congeners. Herein, we demonstrate a trans-azobenzene-based photoregulatory anionophoric system that transports chloride by forming a sandwich dimeric complex. Further studies confirmed a carrier-mediated chloride-anion antiport mechanism, and the supramolecular interactions involved in chloride recognition within the sandwich complex were revealed from theoretical studies. Reversible trans–cis photoisomerization of the azobenzene was achieved without any significant contribution from the thermal cis→trans isomerization at room temperature. Photoregulatory transport activity across the lipid bilayer membrane inferred an outstanding off-on response of the azobenzene photoswitch.     

Graphene Oxide as an Enhancer of Fluorescence

Solvent‐dependent switching of graphene oxide (GO) as fluorescence quencher or enhancer was observed. In some solvents, GO increases the fluorescence yield of a hydrophilic molecule 7‐(diethylamino)‐coumarin‐3‐carboxylic acid (7‐DCA), and in some solvents GO act as a quencher of fluorescence.     

Vibrationally resolved photoionization dynamics of CF4 in the D 2A1 state

Vibrationally resolved photoelectron spectroscopy of the CF4+ (D 2A1) state is studied for the first time over an extended energy range, 26.5相似文献   

π-Hydrogen bonding wins over conventional hydrogen bonding interaction: a jet-cooled study of indole···furan heterodimer

In this study, we have explored the conformational landscape of the indole···furan dimer in a supersonic jet by using resonant two-photon ionization (R2PI) and IR-UV double-resonance spectroscopic techniques combined with dispersion-corrected density functional theory (DFT) calculations. Only one conformer of the dimer has been observed in the experiment. DFT/B97-D level calculation shows that N-H···π hydrogen-bonded conformer (T') is energetically more stable than the N-H···O hydrogen-bonded conformer (HB). Natural bond orbital (NBO) calculation also shows that the hydrogen-bonding interaction in the HB conformer is very weak. Finally, the structure of the observed dimer has been determined to be tilted T-shaped N-H···π hydrogen-bonded (T') from very excellent agreement between experimental and theoretical N-H stretch frequency. The most significant finding of this study is the first-time observation of a N-H···π bound conformer of a dimer, which wins over a conventional hydrogen-bonded conformer of the dimer.     

Determination of Electron and Hole Mobility of Regioregular Poly(3‐hexylthiophene) by the Time of Flight Method

Time of flight method (TOF) is used to measure the electron and hole mobility of a spin coated regioregular poly(3‐hexylthiophene) (P3HT) film. We find that both electron and hole have the same mobility (about 3.8～3.9×10^?4 cm²/Vs) at an applied field of 120 kV/cm. It is demonstrated in this paper that the electron‐hole recombination process may prevent the electron transport in the material due to the fact that the carrier recombination time is much shorter than the transit time.