INVESTIGADORES
AUCAR Gustavo Adolfo
congresos y reuniones científicas
Título:
Invited lecture: Relativistic polarization propagators Novel physical insights and recent applications
Autor/es:
GUSTAVO A. AUCAR
Lugar:
Perugia
Reunión:
Congreso; Computational Theoretical Chemistry EUCO2019; 2019
Institución organizadora:
European Chemical Society
Resumen:
Polarization propagators are theoretical objects that were first developed within the non relativistic, NR, framework in the 1970?s.[1] Their main applications were focused on response properties, like NMR spectroscopic parameters. Its generalization to the relativistic framework was first presented in the early 1990?s [2] and, after another twenty years, they were found to be nicely obtainable from the path integral formalism, from which one can explain some of the previous findings common to both regimes, NR and relativistic.[3] This new formalism is a natural continuation of what is well-known in high-energy physics and so, opened new roads to include QED effects on response properties.In this oral presentation I will show some of the new understandings that arises when using polarization propagators within the relativistic framework. I will focus on the physics that underlies the atomic and molecular response properties, and the way to introduce some of the smallest effects (QED and Gaunt) though measurable by todays experiments, to get accurate theoretical values of NMR spectroscopic parameters. I will also show few of the newest findings, as the likely entanglement between excitations of molecular orbitals.[4]1. P. Jørgensen and J. Oddershede, J. Chem. Phys. 1972, 57, 277; J. Oddershede, Adv. Quantum Chem. 1978, 11, 257.2. G. A. Aucar and J. Oddershede, Int. J. Quantum Chem. 1993, 47, 425; G. A. Aucar, T. Saue, L. Visscher and H. J. Aa. Jensen, J. Chem. Phys. 1999, 110, 6208; G. A. Aucar, A. F. Maldonado, M. D. A. Montero and T. Santa Cruz, Int J Quantum Chem. 2019;119:e25722.3. G. A. Aucar, Phys. Chem. Chem. Phys. 2014, 16, 4420.4. L. A. Millán, C. G. Giribet and G. A. Aucar, Phys. Chem. Chem. Phys. 2018, 20, 24832.