Radially oriented anthracene nanowire arrays: preparation, growth mechanism, and optical fluorescence.

Radially oriented anthracene nanowires and their self-assembled concentric ring arrays were prepared through a facial solvent-evaporation method. The successful growth of anthracene nanowires can be attributed to a combined mechanism of molecular self-assembly facilitated by strong π-π intermolecular interactions together with evaporation-induced capillary flow and fingering instability. Their radial orientation is determined by the capillary flow; their shape (either straight or curved nanowires) is governed by the competition between the capillary and Marangoni convectional flows.

Studies on CuTAPc-nanotube-modified electrodes as chemical sensors for NO.

Poly-copper tetraaminophthalocyanine (CuTAPc) nanotubes were successfully fabricated on porous alumina templates by electropolymerization. Their high surface area and simple preparation protocol made them potential candidates as the modification layer of electrodes for sensor application. High sensitivities and improved linear ranges were obtained through different measurements such as differential pulse voltammetry (DPV), differential potential amperometric (DPA) and electrochemical impedance spectroscopy (EIS).

Fabrication of CuTAPc polymer nanowires and nanotubes by electropolymerization.

Poly-copper tetraaminophthalocyanine (CuTAPc) nanowires and nanotubes were successfully fabricated on porous alumina templates by electropolymerization and characterized using field-emission scanning electron microscopy (FE-SEM), energy-dispersive x-ray spectroscopy (EDX), transmission electron microscopy (TEM) and Raman microscopy. The lengths of these nanostructures could be controlled by the number of cycles applied and the monomer concentrations, while their diameters are confined by the pore size of the template. The product of electropolymerization (whether as nanowires or nanotubes) is a function of the monomer concentrations.

Dry synthesis of triple cumulative double bonds (C=C=C=N) on Si(111)-7 x 7 surfaces.

The interactions of cyanoacetylene and diacetylene with a Si(111)-7 x 7 surface have been studied as model systems to mechanistically understand the chemical binding of unsaturated organic molecules to diradical-like silicon dangling bonds. Vibrational studies show that cyanoacetylene mainly binds to the surface through a diradical reaction involving both cyano and C[triple bond]C groups with an adjacent adatom-rest atom pair at 110 K, resulting in an intermediate containing triple cumulative double bonds (C=C=C=N). On the other hand, diacetylene was shown to the covalently attached to Si(111)-7 x 7 only through one of its C[triple bond]C groups, forming an enynic-like structure with a C=C-C[triple bond]C skeleton.

Synthesis and nonlinear optical absorption of novel porphyrin-osmium-cluster complexes.

Reaction of azido(tetra-p-tolylporphyrinato)indium(III) [TTPInN(3)] and [Os(3)(mu-H)(2)(CO)(10)] in toluene at 80 degrees C overnight gave two major products, complexes 1 and 2. Complex 1 had an axial bridge of "NH", while 2 had an axial bridge of "N" between the porphyrin and osmium cluster moieties. Complex 1 could be converted to 2 when refluxed in toluene.

1,2,3,4-Tetraphenyl-1,2,3,4-tetraphospholane, a highly versatile cyclocarbaphosphine ligand: reactions with activated triosmium clusters and characterization of the products.

Reaction of 1,2,3,4-tetraphenyl-1,2,3,4-tetraphospholane (I) with [Os(3)(CO)(11)(NCMe)] at ambient temperature affords substituted clusters: the monosubstituted trinuclear cluster [Os(3)(CO)(11)[(PPh)(4)CH(2)]] (1) and the isomeric linked bis-trinuclear clusters [[Os(3)(CO)(11)](2)[mu-1,4-eta(2)-(PPh)(4)CH(2)]] (2) and [[Os(3)(CO)(11)](2)[mu-1,3-eta(2)-(PPh)(4)CH(2)]] (3). Clusters 2 and 3 can also be prepared by further reaction of 1 with [Os(3)(CO)(11)(NCMe)]. The reaction at 100 degrees C gives, apart from cluster 2, the disubstituted 1,4-bridged trinuclear cluster [Os(3)(CO)(10)[mu-1,4-eta(2)-(PPh)(4)CH(2)]] (4).