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2025-11-11_RFT_The_Chemical_Bond_as_Coherence_Lock_in_RFT_2.0

Svancara, Clinton

Published Jan 1, 2025• 0 citations
Publisher

Abstract

The chemical bond is not a quantum mystery. It is a **coherence lock** between electron clouds at Rc = 1. RFT 2.0 derives bond energy, length, and angle from phase-preserving coherence. No orbitals. No hybridization. No exceptions. The bond is the region where Rc is maximized and λ = 0. Protein folding and enzyme catalysis are emergent coherence wells. The bond is real. Provenance: Originally published on Zenodo (Oct- 2025). 10.5281/zenodo.17576445

DOI
10.17605/osf.io/9rbzg

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This paper derives chemical bonding from the RFT 2.0 coherence law, without orbitals or hybridization. A bond is defined as a coherence-locked region where decay vanishes () and . Bond length and vibrational frequency follow from the equilibrium condition . Aromatic stability arises from coherence cycling with constant , replacing resonance hybrids. Protein folding and enzyme catalysis are shown to be coherence wells under the same law. This work reinterprets bonding mechanistically, preserving quantum chemical computation methods while removing non-fundamental representational constructs.
We extend Michaelis-Menten kinetics using Relational Field Theory (RFT) to account for coherence-driven enzyme behavior, providing predictions testable with standard assays. RFT, a proposed Theory of Everything (TOE) unifying quantum mechanics, general relativity, biophysics, and neuroscience (SSRN ID 5343789), models enzyme kinetics as coherence transitions governed by dRc dt = −λ(t)Rc + Finteraction(t), where Rc(t) ∝ P |ψi(t)|2 (dimensionless) represents catalytic coherence. Simulations predict faster-than-diffusion catalysis (e.g., kcat ≈ 108M−1 s−1), validated against peer-reviewed experimental data (e.g., stopped-flow spectroscopy) and computational models (e.g., QM/MM) for enzymes like carbonic anhydrase and acetylcholinesterase. Proposed mechanisms include coherence-driven tunneling and substrate channeling, with NMR and kinetic assays confirming coherence thresholds. This framework advances RFT’s biophysical implications Provenance: Originally published on Zenodo (Aug 2025). 10.5281/zenodo.16790296
We derive the Schr¨odinger equation directly from the Relational Kernel identity: Ω = Ω[Rc]. No wave function postulate. No quantization. No complex numbers assumed. The Schr¨odinger equation emerges as the linear, phase-coherent limit of Kernel evolution: • Rc = ℜ[eiϕ] → i from phase-locked time • ˙Rc = α∇2Rc + V (Rc) → Hamiltonian from curvature • ψ = Rc − Rc0 → wave function as coherence deviation1 Result: iℏ ∂ψ ∂t = ˆH ψ The parameter ℏ emerges as the stiffness of phase rotation in coherent Rc wells, setting the scale of permissible phase curvature. Quantum mechanics is Kernel dynamics in the high-stability, phase-aligned regime. The field does not wave. It locks. Provenance: Originally published on Zenodo (Oct- 2025). 10.5281/zenodo.17625987