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Stable modeled

We now generalize our simple illustration. Consider a general transfer function of a stable model G(s), which we also denote as the ratio of two polynomials, G(s) = Q(s)/P(s). We impose a sinusoidal input f(t) = A sin cot such that the output is... [Pg.144]

Silenes and saturated silicon compounds that are coordinated by donors and that thus have higher coordination numbers at the silicon centres exhibit unusual reactivities [1]. An interpretation of these experimental findings is possible when the structural features of the stable model compounds [C6H4CH2N(CH3)2]2SiCl2 (1) [2], [C6H4CH2N(CH3)2]3SiH (4), and [C6H4CH2N(CH3)2]4Si (5) are considered [3]. [Pg.165]

Figure 43. Measuring the importance of parameters. A The distribution of the saturation parameter 0pga (saturation of TPT with respect to PGA) for the full ensemble of models, chosen randomly from the unit interval. B The distribution of the saturation parameter 0pga after restricting the ensemble to stable states only. Within the ensemble of stable models, instances with 0pga close to the linear regime are overrepresented. Figure 43. Measuring the importance of parameters. A The distribution of the saturation parameter 0pga (saturation of TPT with respect to PGA) for the full ensemble of models, chosen randomly from the unit interval. B The distribution of the saturation parameter 0pga after restricting the ensemble to stable states only. Within the ensemble of stable models, instances with 0pga close to the linear regime are overrepresented.
Figure 47. The robustness of metabolic states. Shown is the probability that a randomly chosen state is unstable. Starting with initially 100% stable models, the parameters are subject to increasing perturbations of strength p, corresponding to a random walk in parameter space. (A) The initial states are chosen randomly from the parameter space. (B) The initial states are confined to a small region with 0.01 < < 0. Note that the state Catp exhibits a rapid decay in stability. The data... Figure 47. The robustness of metabolic states. Shown is the probability that a randomly chosen state is unstable. Starting with initially 100% stable models, the parameters are subject to increasing perturbations of strength p, corresponding to a random walk in parameter space. (A) The initial states are chosen randomly from the parameter space. (B) The initial states are confined to a small region with 0.01 < < 0. Note that the state Catp exhibits a rapid decay in stability. The data...
The nature of the transition is finally specified by examining the dissipation of the kinetic energies in stable models, as the pulsation starts with larger amplitudes than their limiting amplitudes. We find that the rates of the dissipation are so small that the pulsation with these amplitudes might be marginally stable. [Pg.193]

The results illustrated so far show that polyreactions in oriented planar monolayers are possible and lead to highly ordered and very stable model membranes. This raises the question whether polymerization is also possible in bilayers (like vesicles and BLM) and whether these bilayers exhibit a higher stability than their unpolymerized counterparts. [Pg.18]

Apart from the possible use of polymerized vesicles as stable models for biomembranes (Sect. 4) there may be a variety of different applications. Polymerized surfactant vesicles have been proposed to act as antitumor agents on a cellular level33 in analogy to the action of the immune system of mammals against tumor cells 85). Polymerized vesicles open the door to chemical membrane dissymmetry 22) which in turn, may lead to enhanced utility in photochemical energy transfer84 (solar energy conversion, artificial photosynthesis). The utilization of unpolymerized lipo-... [Pg.27]

Stable model suspensions of kaolin (Sigma) with average diameter of particles 610 nm as determined by means... [Pg.103]

Wang J, Nation RL, Evans AM, Cox S (2004) Isolated rat kidney perfused with dextran and bovine serum albumin a stable model for investigating renal drug handling. J Pharmacol Toxicol Methods 49 105-113... [Pg.492]

A recognised role for organometallic chemistry is to provide stable models for mechanistic species, thus allowing structural studies to define precisely the geometrical features of the interaction between ligand and transition metal atom. [Pg.5]

In most cases, the MFTA models are built using the Partial Least Squares Regression (PLSR) technique that is suitable for the stable modeling based on the excessive and/or correlated descriptors (under-defined data sets). However, the MFTA approach is not limited to the PLSR models and can successfully employ other statistical learning techniques such as the Artificial Neural Networks (ANN) supporting the detection of the nonlinear structure-activity relationships. ... [Pg.159]

The chemistry of diolefin n complexes of Pd(II) has a special place in the catalytic chemistry of Pd(II) because their reactions with nucleophiles gave adducts that served as stable models for the types of unstable intermediates postulated in many reactions of Pd(II) with olefins. [Pg.425]

Rhodium formate complexes 14 (Scheme 8) have been inferred as possible key intermediates during the catalytic cycle of COj hydrogenation in DMSO/NEtj mixtures . Recently the complexes [ R2P-(X)-PR2 Rh(hfacac)] 13 has been introduced as stable model compounds for 14 Complexes 13a-g were synthesised in order to further improve the catalytic activity by variation of the ligand structure (Table 4). [Pg.136]

Scheme 8 [ R2P-(X)-PR2 Rh(hfacac)J 13 as stable model compounds for rhodium formate... Scheme 8 [ R2P-(X)-PR2 Rh(hfacac)J 13 as stable model compounds for rhodium formate...
Sometimes when model validation is not needed, or to supplement already discussed validity checks, model stability is assessed. Model stability determines how robust the model parameters are to slight changes in the data and how robust the model predictions are to changes in the either the model parameters or input data. Collectively these tests are referred to as sensitivity analysis. If model outputs are particularly sensitive to some parameter then greater accuracy needs to be obtained in estimating that parameter. A stable model is one that is relatively robust to changes in the model parameters and the input data. [Pg.39]

The absorption-enhancing effects of protease inhibitors on the intestinal absorption of water-soluble compounds in rats was also examined. Some protease inhibitors may have absorption-enhancing activities in addition to their protease inhibitory actions (e.g., NaGC) [43, 44]. Aprotinin, bacitracin, and soybean trypsin inhibitor (STI) were used as protease inhibitors, while phenol red and fluorescein isothiocyanate (FITC)-labeled dextran with an average molecular weight of 4000 Da (FD-4) were selected as poorly absorbable and stable model compounds. Bacitracin enhanced the absorption of phenol red from the rat small and large intestine in the presence of the protease inhibitors, and similar results were noted for the intestinal absorption of FD-4 co-administered with bacitracin. Thus, bacitracin was seen to have not only a proteolytic inhibitory action but also an absorption-enhancing capability. [Pg.1472]

In the case of many X variables, principal component analysis (PCA) or partial least squares (PLS) analysis (for reviews, see, e.g., Ref. 52) can be used instead of regression analysis, often leading to more stable models. Both methods are discussed in other chapters of this book (see, e.g., Chapters 22 and 25). [Pg.548]

Wax et al. have studied the hydrogenolysis of ethane over W(100) (79). This surface is itself not active in this reaction until a monolayer of surface carbide is formed, after which an active and very stable model catalyst results. In general, the activity of cleaned metal single crystals for this reaction increased in the order W < Ni < Ru < Ir at the same conditions (573 K, 1 torr ethane, 100 torr H2) (72, 75, 79, 80). [Pg.23]

Kinetic studies of reversible inhibition by substrate analogs give evidence of the mode of action of the inhibitor and the types of enzyme-inhibitor complex formed, and estimates of their dissociation constants. The complexes may be isolated and sometimes crystallized. Studies of the stabilities, optical properties, and structures of ternary complexes of enzymes, coenzymes, and substrate analog in particular, as stable models of the catalytically active ternary complexes or of the transition state for hydride transfer (61,79,109,115-117), can only be touched upon here there is direct evidence with several enzymes that the binding of coenzymes is firmer in such complexes than in their binary complexes (85,93,118), which supports the indirect, kinetic evidence already mentioned for a similar stabilization in active ternary complexes. [Pg.30]

The present study is aimed at investigating the increase in the susceptibility of cellulose towards cellulase in order to increase both rate and yield of sugar. It demonstrates the possibility of regenerating enzyme digested-resistant cellulose into highly susceptible form. It also describes a stable model reaction system for semi- or fully-continuous system for saccharification of cellulose into glucose using untreated culture filtrates of Trichoderma viride. [Pg.434]


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See also in sourсe #XX -- [ Pg.40 , Pg.245 , Pg.246 , Pg.247 , Pg.248 , Pg.249 , Pg.250 , Pg.255 , Pg.256 ]




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