RESUMO
We study quantum systems of volume V, which will exhibit the breaking of a U(1) symmetry in the limit of V-->infinity, when V is large but finite. We estimate the energy difference between the "symmetric ground state" (SGS), which is the lowest-energy state that does not break the symmetry, and a "pure phase vacuum" (PPV), which approaches a symmetry-breaking vacuum as V-->infinity. Under some natural postulates on the energy of the SGS, it is shown that PPVs always have a higher energy than the SGS, and we derive a lower bound of the excess energy. We argue that the lower bound is O(V0), which becomes much larger than the excitation energies of low-lying excited states for a large V. We also discuss the collapse time of PPVs for interacting many bosons. It is shown that the wave function collapses in a microscopic time scale, because PPVs are not energy eigenstates. We show, however, that for PPVs the expectation value of any observable, which is a finite polynomial of boson operators and their derivatives, does not collapse for a macroscopic time scale. In this sense, the collapse time of PPVs is macroscopically long.
RESUMO
We study the robustness, against the leakage of bosons, of wave functions of interacting many bosons confined in a finite box by deriving and analyzing a general equation of motion for the reduced density operator. We identify a robust wave function that remains a pure state, whereas other wave functions, such as the Bogoliubov's ground state and the ground state with a fixed number of bosons, evolve into mixed states. Although these states all have the off-diagonal long-range order, and the same energy, we argue that only the robust state is realized as a macroscopic quantum state.
RESUMO
The synthesis and in vitro antimicrobial activity of a new synthetic carbapenem, (5R,6S)-6-[(R)-1-hydroxyethyl]-2-[(S)-1-acetimidoylpyrrolidin -3-ylthio]-1-carbapen-2-em-3-carboxylic acid (RS-533), are described. The MIC values of related penems and carbapenems are also given for comparison with those of the new carbapenem.
Assuntos
Antibacterianos/síntese química , Tienamicinas/síntese química , Bactérias/efeitos dos fármacos , Indicadores e Reagentes , Espectroscopia de Ressonância Magnética , Testes de Sensibilidade Microbiana , Espectrofotometria Infravermelho , Relação Estrutura-Atividade , Tienamicinas/toxicidadeRESUMO
Cephalosporins possessing a 1, 3-dithiolane, 1, 3-dithiane, or 1, 3-dithietane ring on their 7 beta-substituents showed potent inhibitory activity against cephaloridine hydrolysis by cephalosporinases purified from proteus morganii, Proteus rettgeri, and Proteus inconstans, which were not inhibited by clavulanic acid, a well-known beta-lactamase inhibitor. The mode of inhibition was competitive. The dithiolane cephalosporins themselves were stable against hydrolysis by the beta-lactamases tested. A combination of a dithiolane cephalosporin and cephaloridine synergistically inhibited in vitro growth of strains of P. morganii, P. rettgeri, P. inconstans, Enterobacter aerogenes, Enterobacter cloacae, and Serratia marcescens.
Assuntos
Cefalosporinas/farmacologia , Inibidores de beta-Lactamases , Cefaloridina/farmacologia , Sinergismo Farmacológico , Hidrólise , CinéticaRESUMO
Cephalosporin acylase (EC 3.5.1.11) obtained from Kluyvera citrophila ATCC 21285 was found to catalyze synthesis of 7-[2-(2-thienyl)acetamido]-3-trifluoromethyl-3-cephem-4-carboxylic acid from methyl thienylacetate and dl-7-amino-3-trifluoromethyl-3-cephem-4-carboxylic acid. The enzymatically-synthesized compound showed [alpha]25 D + 42.7 degrees (c 0.058, MeOH) and its biological activity was about twice as much as that of racemic 7-[2-(2-thienyl)acetamidol]-3-trifluoromethyl-3-cephem-4-carboxylic acid chemicall synthesized. As a result, N-acylation by this enzyme was demonstrated to be asymmetric synthesis.