Integrating SMT solvers in Rodin

International audienc

Integrating SMT solvers in Rodin

International audienc

SMT solvers for Rodin

The original publication is available at www.springerlink.comInternational audienceFormal development in Event-B generally requires the validation of a large number of proof obligations. Some automatic tools exist to automatically discharge a significant part of them, thus augmenting the efficiency of the formal development. We here investigate the use of SMT (Satisfiability Modulo Theories) solvers in addition to the traditional tools, and detail the techniques used for the cooperation between the Rodin platform and SMT solvers. Our contribution is the definition of two approaches to use SMT solvers, their implementation in a Rodin plug-in, and an experimental evaluation on a large sample of industrial and academic projects. Adding SMT solvers to Atelier B provers reduces to one fourth the number of sequents that need to be proved interactively

SMT solvers for Rodin ⋆

Abstract. Formal development in Event-B generally requires the validation of a large number of proof obligations. Some automatic tools exist to automatically discharge a significant part of them, thus augmenting the efficiency of the formal development. We here investigate the use of SMT (Satisfiability Modulo Theories) solvers in addition to the traditional tools, and detail the techniques used for the cooperation between the Rodin platform and SMT solvers. Our contribution is the definition of two approaches to use SMT solvers, their implementation in a Rodin plug-in, and an experimental evaluation on a large sample of industrial and academic projects. Adding SMT solvers to Atelier B provers reduces to one fourth the number of sequents that need to be proved interactively.

Design of new sensitive α,β-unsaturated carbonyl 1,8-naphtalimide fluorescent probes for thiol bioimaging

International audienceWe report herein an efficient synthesis of news naphtalimide-based fluorescent derivatives functionalized with an a,(3-unsaturated carbonyl group. Probes were synthesized from reaction of an amino-naphtalimide precursor with maleic anhydride. Photophysical study of fluorescent probes and cells labelling were performed, and showed that the reactive derivatives exhibit rich turn on fluorescence properties in presence of different biological thiol (Glutathione and Cysteine) making these systems a very promising way for thiol bioimaging