J-aggregates of the diacid form of tetra(p-hydroxyphenyl)porphyrin (THPP) were found to be stable in nonionic micellar solution in the presence of trace ionic surfactant with an oxyacid headgroup. The excitation energy of exciton coupling depends systematically on the headgroups of the ionic surfactant, by which strong and weak coupling can be accomplished in the J-aggregates. The J-aggregates have two strong exciton bands corresponding to the B- and Q-bands of the protonated monomers. The total fluorescence of THPP is quenched through aggregate formation. A strong and sharply peaked resonance light-scattering signal that suggests a delocalized excitonic state was observed just slightly to the red of the absorption maximum of the J-aggregates. The overall resonance Raman intensities appeared to be stronger in the aggregates than in the monomers. In the kinetics of aggregation induced by sodium dodecyl sulfate (SDS), no characteristics of autocatalyzed reactions were observed, and there was only a logarithmic phase that lasted only several seconds.

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This paper focuses on the passive control problem for Markov jump systems with piecewise-constant transition rates, random nonlinearities and random communication delays. An observer is used to obtain the system state, and communication delay with probabilistic distribution is considered. The probabilistic properties of the nonlinear perturbations and communication delays are described by two mutually independent Bernoulli sequences. Based on average dwell time method and Lyapunov stability theory, a sufficient stochastic passivity condition is presented. By singular value decomposition technique the gain matrices can be computed via strict linear matrix inequalities, and the desired controller guarantees the stochastic passivity of the closed-loop augmented system. The effectiveness of the method is illustrated by a numerical example.

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The interactions of nonionic meso-tetra(p-hydroxyphenyl)porphyrin (THPP) with CX3COOH (X = F, Cl, Br) in Triton X-100 (TX) micellar solution have been investigated by optical absorption, resonance light-scattering, and fluorescence spectroscopies. The double red-shifted absorption bands and strong resonance light scattering (RLS) signal imply that the assemblies induced by trihalo acetic acids belong to J-aggregates. The fluorescence of porphyrin is quenched due to the aggregate formation. The kinetics of assemblies trigged by CBr3COOH is studied via stopped-flow techniques. No characteristics of autocatalyzed reactions are observed, and there is only a log phase. The nature of the exciton coupling of transition dipole moment can be systematically changed by the haloid substituents of the organic counteranion.