A Model for Information Processing Capacity: Formalizing the Impact of Structural and Information System Choices on Organizational Performance

This paper proposes a formal model of information processing inorganizations. The model takes a process view of organizations and includesboth structural and IS features of processes. Two structural properties areconsidered, networking and parallelism. Information systems are representedin terms of quantity of information used and level of informationcustomization allowed. Process performance is measured in terms of totalinformation processing capacity and flexibility afforded by a process. Therelationship between structural and information system choices and processperformance is studied by simulating the model for a range of values. Thepaper derives a set of propositions describing the independent and combinedimpact of structural and information system choices on performance. The results suggest the predominance of networking over parallelism and ofinformation customization over information quantity in determininginformation processing capacity. They also show a negative effect ofnetworking on process flexibility and an amplifying effect of networking onthe benefits of information customization. Overall, the findings validatethe interdependence between structural and information system variables indetermining process performance.     

Synthesis,photoluminescence, and electrochromism of novel aromatic poly(amine‐1,3,4‐oxadiazole)s bearing anthrylamine chromophores

Two novel poly(amine‐hydrazide)s were prepared from the polycondensation reactions of the dicarboxylic acid, 9‐[N,N‐di(4‐carboxyphenyl)amino]anthracene ( 1 ), with terephthalic dihydrazide ( TPH ) and isophthalic dihydrazide ( IPH ) via the Yamazaki phosphorylation reaction, respectively. The poly(amine‐hydrazide)s were readily soluble in many common organic solvents and could be solution cast into transparent films. Differential scanning calorimetry (DSC) indicated that these hydrazide polymers had glass‐transition temperatures (T_g) in the range of 182–230 °C and could be thermally cyclodehydrated into the corresponding oxadiazole polymers in the range of 300–400 °C. The resulting poly(amine‐1,3,4‐oxadiazole)s had useful levels of thermal stability associated with high T_g (263–318 °C), 10% weight‐loss temperatures in excess of 500 °C, and char yield at 800 °C in nitrogen higher than 55%. These organo‐soluble anthrylamine‐based poly(amine‐hydrazide)s and poly (amine‐1,3,4‐oxadiazole)s exhibited maximum UV‐vis absorption at 346–349 and 379–388 nm in N‐methyl‐2‐pyrrolidone (NMP) solution, respectively. Their photoluminescence spectra in NMP solution showed maximum bands around 490–497 nm in the green region. The poly(amine‐hydrazide) I ‐ IPH showed a green photoluminescence at 490 nm with PL quantum yield of 29.9% and 17.0% in NMP solution and film state, respectively. The anthrylamine‐based poly(amine‐1,3,4‐oxadiazole)s revealed a electrochromic characteristics with changing color from the pale yellow neutral form to the red reduced form when scanning potentials negatively from 0.00 to ?2.20 V. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 1584–1594, 2009     

Poly(arylene sulfide)s by nucleophilic aromatic substitution polymerization of 2,7‐difluorothianthrene

Poly(thianthrene phenylene sulfide) and poly(thianthrene sulfide) have been prepared by nucleophilic aromatic substitution polymerization of the activated monomer 2,7‐difluorothianthrene with bis thiophenoxide and sulfide nucleophiles, respectively. The resulting polymers are thermally stable, amorphous materials that have been characterized by differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), gel permeation chromatography (GPC), matrix‐assisted laser desorption/ionization‐time‐of‐flight (MALDI‐TOF) mass spectrometry, UV‐Vis spectroscopy, refractometry, and intrinsic viscosity (IV) measurements. The polymers produced exhibit 5% weight loss values approaching 500 °C in inert and air atmospheres and glass transition temperatures that range from 149 to 210 °C. Poly(thianthrene phenylene sulfide) with a number average molecular weight of 22,100 g/mol has been synthesized with an IV in DMPU of 0.62 dL/g at 30 °C. Creasable films of this polymer have been prepared by solvent casting and melt pressing at 250 °C. Films of poly(thianthrene phenylene sulfide) exhibit transparencies greater than 50% at wavelengths exceeding 400 nm and a high refractive index value of 1.692 at a wavelength of 633 nm, making the polymer interesting for optical applications. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 2453–2461, 2009     

Determination of tectoridin in rat plasma by high‐performance liquid chromatography and its application to pharmacokinetic studies

A simple, specific and sensitive HPLC method with UV detection was developed and validated for the determination of tectoridin in rat plasma for the first time. Chromatographic separation was performed on a Welchrom^TM C₁₈ column (150 × 4.6 mm, i.d., 5 µm) at a flow rate of 1.0 mL min^?1, using a mixture of methanol–2% HAc aqueous solution (31:69, v/v) as the mobile phase with UV detection at 266 nm. The calibration curves for tectoridin were linear over the concentration range of 1.10–274.40 µg mL^?1 in rat plasma. The intra‐ and inter‐day accuracies (RE) were within ?3.23% and 4.11%. The intra‐ and inter‐day precisions (RSD) were not more than 2.74 and 4.72%, respectively. The present method was successfully applied to the pharmacokinetic studies of tectoridin in rats after intravenous administration of three different doses. Copyright © 2009 John Wiley & Sons, Ltd.     

Portfolio selection under strict uncertainty: A multi-criteria methodology and its application to the Frankfurt and Vienna Stock Exchanges

In modern portfolio theory, it is common practice to first compute the risk-reward efficient frontier and then to support an individual investor in selecting a portfolio that meets his/her preferences for profitability and risk. Potential flaws include (a) the assumption that past data provide sufficient evidence for predicting the future performances of the securities under consideration and (b) the necessity to mathematically determine or approximate the investor’s utility function. In this paper, we propose a methodology whose initial phase filters portfolios that are inefficient from a historical perspective. While this is consistent with traditional approaches, the second phase differs from the standard approach as it uses a decision table constructed by considering multiple scenarios assuming strict uncertainty. The table cells measure consequences by a multi-criteria linear performance index of simulated future returns, which avoids difficulties with performance ratios. The real world applicability is illustrated through two studies based on data from the stock exchanges in Frankfurt and Vienna.     

Nonlinear optimization with GAMS /LGO

The Lipschitz Global Optimizer (LGO) software integrates global and local scope search methods, to handle a very general class of nonlinear optimization models. Here we discuss the LGO implementation linked to the General Algebraic Modeling System (GAMS). First we review the key features and basic usage of the GAMS /LGO solver option, then present reproducible numerical results to illustrate its performance.     

最大顶点覆盖问题的一种近似算法

给出了求解最大顶点覆盖问题的一种近似算法,讨论了它的性能保证,利用P ipage技术,为最大顶点覆盖问题设计出了0.75-近似算法.     

Synthesis of phenylquinoxaline oligomers containing pendant electron‐donating and electron‐withdrawing groups

A series of extended 6‐substituted quinoxaline AB monomer mixtures, 2‐(4‐fluorophenyl)‐3‐[4‐(4‐hydroxyphenoxy)phenyl]‐6‐substituted quinoxaline and 3‐(4‐fluorophenyl)‐2‐[4‐(4‐hydroxyphenoxy)phenyl]‐6‐substituted quinoxaline, were prepared and polymerized to afford phenylquinoxaline oligomers. High‐molecular‐weight polymers could not be obtained because of the formation of cyclic oligomers. On the basis of matrix‐assisted laser desorption/ionization time‐of‐flight analysis and molecular modeling results, the formation of a cyclic dimer could be a favorable process resulting in low‐molecular‐weight oligomers. They were completely soluble and amorphous, with glass‐transition temperatures varying from 165 to 266 °C, and they had thermooxidative stability, with samples displaying 5% weight loss temperatures of 419–511 °C in nitrogen. The thermal properties of the monomers and resultant polymers dramatically depended on the polarity of the substituents. The monomers and resultant oligomers displayed high fluorescence in tetrahydrofuran solutions and N‐methyl‐2‐pyrrolidinone solutions, respectively. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 6465–6479, 2005     

Comparative analysis of the effects of internal lasing oscillation and external light injection on semiconductor optical amplifier performance

One of the key differences of a semiconductor optical amplifier (SOA) with internal lasing oscillation (ILO) from a SOA with external light injection (ELI) lies in a carrier-sharing mechanism. Since the internal lasing mode shares the same pool of carriers with the signals, the carriers (or photons) withdrawn from the circulating laser mode speed up the gain recovery. On the other hand, the external light injected into the SOA shortens the carrier recovery time through optical pumping without any carrier sharing involved. To find out a better scheme, we have made a comparative investigation on the effects of the ILO and ELI on the SOA performance. It turns out by way of simulation that the ELI scheme provides faster gain recovery, shorter carrier lifetime, and higher saturation power when the external injection power is higher than the internal lasing power. The performance enhancement is not so pronounced with the carrier-sharing mechanism, as the internal lasing mode itself gives rise to severe longitudinal spatial hole burning (LSHB). Nevertheless, the ILO scheme is preferable for linear-amplification applications. We also examine the use of the ELI for low-crosstalk optical amplifiers. It is found that the ELI scheme does not bring in a very strong resonance peak in the crosstalk, which appears in a SOA with ILO due to relaxation oscillations of the lasing mode. In comparison to the ILO in SOAs, the ELI into SOAs is likely to leave more optical gain for multi-channel amplification without any sacrifice on the crosstalk.