Integrated CMOS system and thermally actuated optical switch for wavelength modulation/lock in communication network

The advancement of communication technology and growth of internet traffic have continuously driven the fast evolution of networks. Compared to the traditional optoelectronic switch, all-optical switch provides high throughput, rich routing functionalities, and excellent flexibility for rapid signal exchange in fiber optical network. Among various all-optical switches, thermal actuated ring switch provides the advantages of high accuracy, easy actuation, and reasonable switching speed. However, when scale up, thermal ring switch may encounter issues related to fabrication error, non-accurate wavelength response, and large terminal numbers in the control circuit. In this research, we propose the employment of an integrated CMOS control circuit to compensate the fabrication error and tune as well as lock the wavelength in a thermal-actuated ring-type optical switch through a frequency modulation scheme. Additional functionalities can also be added in this circuit by tailoring externally the roundtrip loss or coupling constants of the ring. The design concept can be easily scaled up for large array optical switch system without much change in the terminal numbers thanks to the three-dimensional hierarchy of control circuit design, which effectively reduces the terminal numbers into the cubic root of the total control unit numbers. The integrated circuit has been designed, simulated, as well as fabricated, and demonstrated a decent performance with free spectral range (FSR) equal to 1.5 nm at 1534 nm and very accurate wavelength modulation to 0.3 nm within 0.01 nm fluctuation for thermal actuated ring type optical switch.     

Enhancement of Anticancer Potential of Pterostilbene Derivative by Chalcone Hybridization

Pterostilbene, a natural metabolite of resveratrol, has been indicated as a potent anticancer molecule. Recently, several pterostilbene derivatives have been reported to exhibit better anticancer activities than that of the parent pterostilbene molecule. In the present study, a series of pterostilbene derivatives were designed and synthesized by the hybridization of pterostilbene, chalcone, and cinnamic acid. The cytotoxic effect of these hybrid molecules was determined using two oral cancer cell lines, HSC-3 and OECM-1. (E)-3-(2-((E)-4-Hydroxystyryl)-4,6-dimethoxyphenyl)-1-(2-methoxyphenyl)prop-2-en-1-one (4d), with IC₅₀ of 16.38 and 18.06 μM against OECM-1 and HSC-3, respectively, was selected for further anticancer mechanism studies. Results indicated that compound 4d effectively inhibited cell proliferation and induced G2/M cell cycle arrest via modulating p21, cyclin B1, and cyclin A2. Compound 4d ultimately induced cell apoptosis by reducing the expression of Bcl-2 and surviving. In addition, cleavage of PARP and caspase-3 were enhanced following the treatment of compound 4d with increased dose. To conclude, a number of pterostilbene derivatives were discovered to possess potent anticancer potentials. Among them, compound 4d was the most active, more active than the parent pterostilbene.     

双相不锈钢在水溶液中之腐蚀疲劳与动态应变时效

本研究主要探讨 2 2 %Cr双相不锈钢在含氯离子水溶液中之腐蚀疲劳裂缝成长行为 ,以及在慢应变速率拉伸试验过程中所发生的动态应变时效现象 .同时以 31 6L沃斯田体系不锈钢及4 30肥粒体系不锈钢作为比较 ,藉以探讨不同晶体结构对腐蚀疲劳及动态应变时效行为的影响 .实验结果显示 ,在 80℃ ,3.5wt%NaCl水溶液中 ,3种不锈钢并未发生应力腐蚀破裂 ,但其中 31 6L沃斯田体系不锈钢及 2 2 %Cr双相不锈钢却发生动态应变时效 ,且动态应变时效的发生与温度 ,应变速率及沃斯田体相的组织有关 .在NaCl水溶液中 ,采用预裂试片量测疲劳裂缝生长速率 ,其结果表明 ,4 30肥粒体系不锈钢之疲劳裂缝生长速率最快 ,而氢脆是加快裂缝生长速率的主因 ,就双相不锈钢而言 ,腐蚀疲劳裂缝的生长主要与该不锈钢所含之肥粒体相的氢脆现象有关     

Total Synthesis of Carpacin and its Geometric Isomer as a Cancer Chemopreventer

Carpacin ( 1a ), an antidepressant in Asiatic folk medicine from the Carpano tree, is achieved in which the longest linear sequence is only four steps in over all yield 67% from commercially available Sesamol. The key transformations in the synthesis are the selective palladium‐catalyzed coupling reactions of aryl bromide with Grignard reagents. The first preparation of its geometric isomer ( 1b ) is described. Highlights of the synthesis include Pd‐catalyzed coupling, selective hydrogenation, and Wittig reactions. Carpacin was examined as a potential inhibitor of carcinogenesis.     

An ε-relaxation method for separable convex cost generalized network flow problems

We generalize the ε-relaxation method of [14] for the single commodity, linear or separable convex cost network flow problem to network flow problems with positive gains. The method maintains ε-complementary slackness at all iterations and adjusts the arc flows and the node prices so as to satisfy flow conservation upon termination. Each iteration of the method involves either a price change on a node or a flow change along an arc or a flow change along a simple cycle. Complexity bounds for the method are derived. For one implementation employing ε-scaling, the bound is polynomial in the number of nodes N, the number of arcs A, a certain constant Γ depending on the arc gains, and ln(ε⁰/), where ε⁰ and denote, respectively, the initial and the final tolerance ε. Received: November 10, 1996 / Accepted: October 1999?Published online April 20, 2000     

Co-NP-completeness of some matrix classification problems

The classes of P-, P ₀-, R ₀-, semimonotone, strictly semimonotone, column sufficient, and nondegenerate matrices play important roles in studying solution properties of equations and complementarity problems and convergence/complexity analysis of methods for solving these problems. It is known that the problem of deciding whether a square matrix with integer/rational entries is a P- (or nondegenerate) matrix is co-NP-complete. We show, through a unified analysis, that analogous decision problems for the other matrix classes are also co-NP-complete. Received: April 1999 / Accepted: March 1, 2000?Published online May 12, 2000     

Mesoporous Silica Promoted Deposition of Bioinspired Polydopamine onto Contrast Agent: A Universal Strategy to Achieve Both Biocompatibility and Multiple Scale Molecular Imaging

Polydopamine (PDA) preserves universal coating and metal‐binding ability, and is suitable for application in synthesizing multifunctional agents. Herein, utilizing mesoporous silica assisted deposition to enhance both heterogeneous nucleation and loading amounts of PDA, the magnetic resonance (MR) T₁ component (PDA‐Fe³⁺) and MR T₂/computed tomography (CT)/multiphoton luminescence (MPL) component (FePt) have been successfully integrated in aqueous solution. This four‐in‐one (T₁, T₂, CT, MPL) imaging nanocomposite, FePt@mSiO₂ @PDA‐polyethylene glycol (PEG), demonstrated its multi‐imaging power both in vitro/in vivo. According to our in vitro/in vivo results, FePt@mSiO₂@PDA‐PEG reveals water‐content‐dependent property in T₁ MR imaging, which suggests the necessity of having dual‐modal MR ability in a single particle for the precision diagnosis. Most importantly, this dual (T₁,T₂)‐MRI/CT contrast agent is demonstrated complementary to each other in the in vivo testing. PDA coated mesoporous silica also offers an advantage of delayed degradation that prevents adverse effects caused by silica fragments before excretion. The potential of this nanocomposites in both drug carrier and photothermal agent was further evaluated by using doxorubicin and monitoring solution temperature after irradiating 808 nm continuous‐wave, respectively The merits of controlled polymerization, enhanced PDA loading, and biofavorable degradation make this methodology promising to other nanoparticle@mSiO₂ for a wide range of bioapplications.     

A photoactive molecular triad as a nanoscale power supply for a supramolecular machine

A tetrathiafulvalene-porphyrin-fullerene (TTF-P-C(60)) molecular triad, which generates electrical current by harnessing light energy when self-assembled onto gold electrodes, has been developed. The triad, composed of three unique electroactive components, namely, 1) an electron-donating TTF unit, 2) a chromophoric porphyrin unit, and 3) an electron-accepting C(60) unit, has been synthesized in a modular fashion. A disulfide-based anchoring group was tagged to the TTF end of the molecule in order to allow its self-assembly on gold surfaces. The surface coverage by the triad in a self-assembled monolayer (SAM) was estimated to be 1.4 nm(2) per molecule, a density which is consistent with hexagonal close-packing of the spherical C(60) component (diameter approximately 1 nm). In a closed electronic circuit, a triad-SAM functionalized working-electrode generates a switchable photocurrent of approximately 1.5 microA cm(-2) when irradiated with a 413 nm Kr-ion laser, a wavelength which is close to the porphyrin chromophore's absorption maximum peak at 420 nm. The electrical energy generated by the triad at the expense of the light energy is ultimately exploited to drive a supramolecular machine in the form of a [2]pseudorotaxane comprised of a pi-electron-deficient tetracationic cyclobis(paraquat-p-phenylene) (CBPQT(4+)) cyclophane and a pi-electron-rich 1,5-bis[(2-hydroxyethoxy) ethoxy]naphthalene (BHEEN) thread. The redox-induced dethreading of the CBPQT(4+) cyclophane from the BHEEN thread can be monitored by measuring the increase in the fluorescence intensity of the BHEEN unit. A gradual increase in the fluorescence intensity of the BHEEN unit concomitant with the photocurrent generation, even at a potential (0 V) much lower than that required (-300 mV) for the direct reduction of the CBPQT(4+) unit, confirms that the dethreading process is driven by the photocurrent generated by the triad-SAM.     

Formosadimers A, B, and C from the Bark of Calocedrus macrolepis var. formosana

Formosadimers A, B, and C, together with one known compound, sugikurojin B, have been isolated from the bark of Calocedrus macrolepis var. formosana. Formosadimers A, B, and C, and sugikurojin B are dimers of the abietane-O-abietane type. Their structures were elucidated principally based on spectroscopic data.