Thermomagnetic effect in ferrofluids with weakly coupled particles

Thermomagnetic curves for water based ferrofluid with large magnetic latex particles are analyzed. The particles are found to have extremely low barrier height of thermal relaxation (≤1200 K at temperatures below 100 K) whose field dependence is deduced. Work sponsored by the National Science Council of the R.O.C. under Grant No. NSC85-2112-M-001-020.     

Synthesis and optical and electrochemical properties of copolymers consisting of 9,9‐dihexylfluorene and aromatic triazole chromophores

Aromatic triazole chromophores were incorporated into polyfluorene in an attempt to increase electron affinity, to promote emission efficiency, and to diminish excimer formation. Poly(9,9‐dihexylfluorene) ( P1 ) and new copolymers with aromatic triazoles ( P2 – P4 ) were prepared by Suzuki coupling polymerization. In P2 , the aromatic triazole (3.8 mol %) was attached exclusively as terminal groups, whereas P3 and P4 were main‐chain copolymers containing 3.9 and 10.3 mol % aromatic triazole chromophores, respectively. The copolymers were soluble in common organic solvents and showed high decomposition temperatures (437–458 °C). The twisted structure between the triazole and fluorene increased the emission efficiency and effectively prevented excimer formation in P2 – P4 . After the introduction of the triazole units, the absorption spectra showed a blueshift (from 388 to 381 nm in chloroform) due to confined conjugation, but the photoluminescence spectra remained almost the same (417–418 nm); this was attributed to oligofluorene segments. No emission of triazole fluorophores was observed because of efficient energy transfer from the triazole to oligofluorene segments. However, incomplete energy transfer was observed in CH₃COOH. The optical stability upon thermal annealing was also improved by the incorporation of aromatic triazole segments. From cyclic voltammetry results, P2 – P4 , containing triazole groups, showed greater electron affinity (lowest unoccupied molecular orbital level = ?2.67 to ?2.71 eV) than P1 (?2.52 eV). Electroluminescence devices of P1 – P4 all exhibited excimer emissions (483–521 nm), which could also be diminished by the introduction of aromatic triazole chromophores. © 2006Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 136–146, 2007     

Optical and electrochemical properties of copoly(aryl ether)s consisting of alternate 2,5‐distyrylbenzene and electron‐transporting oxadiazole or triazole derivatives

New copoly(aryl ether) P1 consisting of alternate electron‐transporting 2‐(3‐(trifluoromethyl)phenyl)‐5‐(4‐(5‐(3‐(trifluoromethyl)phenyl)‐1,3,4‐oxadiazol‐2‐yl)‐2,5‐bis(hexyloxy)phenyl)‐1,3,4‐oxadiazole and hole‐transporting 2,5‐distyrylbenzene (DSB) was synthesized via nucleophilic substitution polymerization. We investigated the optical and electrochemical properties of alternate copoly(aryl ether)s P1 – P6 , which contain the same hole‐transporting DSB segments, but with different electron transporting segments. The effect of trifluoromethyl groups in electron transporting segments is also discussed. Referencing to the spectra of their model compounds M1 – M4 , the emissions of P1 – P3 are dominated exclusively by the hole‐transporting fluorophores with longer emissive wavelength about 452–453 nm via efficient excitation energy transfer. Furthermore, P1 – P3 also exhibit unique variations in energy transfer in acidic media and solvatochromism in organic solvents. The highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO) energy levels of P1 – P4 , estimated from electrochemical data, are ?5.12, ?5.15, ?5.18, ?5.00 eV and ?2.93, ?3.39, ?3.49, ?2.76 eV, respectively. The electron and hole affinity of P1 – P6 can be enhanced simultaneously by introducing isolated hole‐ and electron‐transporting segments in backbone. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 5083–5096, 2005     

Cheating in Visual Cryptography

A secret sharing scheme allows a secret to be shared among a set of participants, P, such that only authorized subsets of P can recover the secret, but any unauthorized subset cannot recover the secret. In 1995, Naor and Shamir proposed a variant of secret sharing, called visual cryptography, where the shares given to participants are xeroxed onto transparencies. If X is an authorized subset of P, then the participants in X can visually recover the secret image by stacking their transparencies together without performing any computation. In this paper, we address the issue of cheating by dishonest participants, called cheaters, in visual cryptography. The experimental results demonstrate that cheating is possible when the cheaters form a coalition in order to deceive honest participants. We also propose two simple cheating prevention visual cryptographic schemes.     

Aryne‐Induced Novel Tandem 1,2‐Addition/(3+2) Cycloaddition to Generate Imidazolidines and Pyrrolidines

A new “single‐flask” method was developed for the synthesis of imidazolidines and pyrrolidines with high stereoselectivity. First, a Schiff base was arylated with an aryne. Second, an intramolecular proton transfer took place from the methylene position to the anionic aryne ring. Third, the resultant ylide reacted with a second equivalent of the same Schiff base in situ or an electron‐deficient alkene through a (3+2) cycloaddition. These sequential tandem 1,2‐addition/(3+2) cycloaddition reactions led to the desired heterocycles in 63–88 % yields.     

Influence of organoclay dispersed state of poly(ethylene glycol‐co‐1,3/1,4‐cyclohexanedimethanol terephthalate)/organoclay nanocomposites on their characteristics

This work prepared poly(ethylene glycol‐co‐1,3/1,4‐cyclohexanedimethanol terephthalate) (PETG)/organoclay nanocomposites via a melt intercalation process and investigated the influences of organoclay aspect ratio and organoclay content on the dispersed state, mechanical, thermal, gas barrier, and heat recovery properties of PETG/organoclay nanocomposites. X‐ray diffraction (XRD) and transmission electron microscopic analyses showed that the organoclay dispersed in the polymer matrix with intercalation in the nanometer scale range. Differential scanning calorimetry (DSC) analysis demonstrated that all of the obtained nanocomposites were amorphous, indicating that the addition of organoclay did not affect the amorphous nature of PETG. The gas barrier properties of the nanocomposites improved with organoclay content and the properties were also affected by the organoclay aspect ratio. Water vapor and oxygen transmission rates (OTRs) of PETG/organoclay nanocomposites containing 3 phr Cloisite 15A, and 3 phr modified polymer grade Na‐montmorillonites (MPGN) were the lowest among the samples tested, and were 41.7 and 44.3%, respectively, of those of neat PETG. Similar organoclay content‐ and aspect ratio‐related effects were observed in the mechanical and heat recovery properties of the tested nanocomposites. Copyright © 2010 John Wiley & Sons, Ltd.     

Varactor-tuned gunn diode voltage controlled oscillator antenna array

A simple varactor tuned X-band Gunn diode VCO antenna array which is strongly coupled has been demonstrated. These arrays have the advantages of simple biasing circuit, no resistors required to eliminate multimode problem and suitable for monolithic integration circuit. Preliminary results show a maximum tuning range of 47MHz for 1×1 array and 170MHz for 2×2 array. In order to solve power combining heating problem, we move the backside metal forward and it becomes a microstrip form. The measured frequency and radiation patterns of these grid arrays agree very well with theoretical calculations.     

Epitaxial growth in the (111)Ag/Cu and (111)Au/Cu systems

The initial stages of epitaxial growth in the (111)Ag/Cu and (111)Au/Cu systems were investigated using UHV-RHEED and TEM on the same specimens. Flat, monocrystalline (111)Cu substrates, 1100 Å thick, were formed in situ in the RHEED system on (111)NaCl/mica bilayers. The latter consisted of air-cleaved mica on which 150 Å of NaCl was vacuum-evaporated to form a (111)NaCl monocrystalline film. The NaCl layer allowed easy removal in water of the subsequently deposited bilayer metal film. RHEED showed that these Cu films grew with extremely flat surfaces at 400°C and 10 Å/sec deposition rates. They were then annealed at 500°C for 15 min to reduce their dislocation content and finally used as substrates for subsequent deposition of thin Ag or Au superlayers. The average Ag and Au superlayer thicknesses were varied from fractions of an Angstrom to approximately 20 Å. It was shown that despite the elongated streaks in the RHEED patterns, film growth occurred by an island mechanism, the islands having flat top surfaces. In the initial growth processes, the islands merely thickened. After a few average monolayers were deposited, the islands began to widen, often by means of much thinner islands, finally coalescing into a continuous film. The Au overgrowths became continuous in the 6–11 Å thickness range. In the case of Ag, there still were some open areas in the overgrowth at 20 Å. In both cases the continuous regions of the Ag and Au overgrowths consisted of sharply delineated thick and thin areas that gave rise to steps on the otherwise flat surface.