Quantum Indistinguishability in Chemical Reactions
Matthew P. A. Fisher, Leo Radzihovsky

TL;DR
This paper emphasizes the importance of quantum indistinguishability in chemical reactions involving symmetric molecules, proposing a Quantum Dynamical Selection rule that impacts reactivity, entanglement, isotope fractionation, and biological quantum processes.
Contribution
It introduces the Quantum Dynamical Selection rule for symmetric molecules, highlighting the necessity of quantum treatment in chemical reactions traditionally modeled classically.
Findings
Differential reactivity of para- and ortho-hydrogen
Mechanism for inter-molecular nuclear spin entanglement
New isotope fractionation mechanism
Abstract
Quantum indistinguishability plays a crucial role in many low-energy physical phenomena, from quantum fluids to molecular spectroscopy. It is, however, typically ignored in most high temperature processes, particularly for ionic coordinates, implicitly assumed to be distinguishable, incoherent and thus well-approximated classically. We explore chemical reactions involving small symmetric molecules, and argue that in many situations a full quantum treatment of collective nuclear degrees of freedom is essential. Supported by several physical arguments, we conjecture a "Quantum Dynamical Selection" (QDS) rule for small symmetric molecules that precludes chemical processes that involve direct transitions from orbitally non-symmetric molecular states. As we propose and discuss, the implications of the Quantum Dynamical Selection rule include: (i) a differential chemical reactivity of para-…
Peer Reviews
No public reviews on file for this paper yet. If you reviewed it on a platform where reviews are public (OpenReview, ICLR, NeurIPS, ICML), you can paste yours below so the community can read it here.
Videos
No videos yet. Explain this paper in a talk, walkthrough, or lecture? Add one.
