Emergent Assembly Chirality and Flip Kinematics: Euclidean Stabilizers of the Frame Classes, Enantiotopic Faces of the C2h Core, and Initiator Capping of the Interior Lattice

The canonical planar chrysene carbon framework has point group $C_{2h}$ and no reflection symmetry within its plane. We establish that its locant involution is induced by the in-plane half-turn $C_2(z)$; no proper face-exchanging rotation preserves the same carbon footprint. We then separate the finite registry classification from its geometric realization. Under an explicit faithful, reflection-equivariant decorated-realization hypothesis, a species-symmetric stack is achiral precisely when its alignment field is palindromic. At length $l=6$, the $32$ fields comprise $8$ achiral fields and $24$ chiral fields forming $12$ mirror pairs. Uniform endogenous draws are racemic at the ensemble level, whereas ideal placement can select one member of a pair. A unique asymmetric terminal cap removes the candidate nonidentity stabilizers under the stated layer-preservation and realization conditions. The imported matched-source model yields an initiator surplus of $19.8$ units per period, exceeding the separate resource demands of $1$, $9$, or $18$ caps; saturated in-layer placement is available only on the compatible boundary columns, while other columns require external overhangs. Finally, a finite arm-sign model partitions the $D$ and $T$ states by stabilizer and gives an explicit orientation bias for fixed, identical anti or mixed states. Thermal restoration of blindness follows from invariance of the joint conformational measure under a single-partner half-turn. A correlated anti-state counterexample shows why symmetric one-unit marginals alone do not suffice. Exact enumeration, new verification code, and finite Lean certificates support the algebraic statements; the geometric and chemical interpretation is stated through explicit realization assumptions.

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Publication Details

Journal
Annals of the Chrysene Formalism
Published
2026-11-06
DOI
https://doi.org/10.68366/r2wxe526
Primary Topic
Chemistry and Stereochemistry Studies
Type
article
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article

Emergent Assembly Chirality and Flip Kinematics: Euclidean Stabilizers of the Frame Classes, Enantiotopic Faces of the C2h Core, and Initiator Capping of the Interior Lattice

Charles D. Schaper
1 links
Annals of the Chrysene Formalism
Chemistry and Stereochemistry Studies
article

Emergent Assembly Chirality and Flip Kinematics: Euclidean Stabilizers of the Frame Classes, Enantiotopic Faces of the C2h Core, and Initiator Capping of the Interior Lattice

Charles D. Schaper
article en

Abstract

The canonical planar chrysene carbon framework has point group $C_{2h}$ and no reflection symmetry within its plane. We establish that its locant involution is induced by the in-plane half-turn $C_2(z)$; no proper face-exchanging rotation preserves the same carbon footprint. We then separate the finite registry classification from its geometric realization. Under an explicit faithful, reflection-equivariant decorated-realization hypothesis, a species-symmetric stack is achiral precisely when its alignment field is palindromic. At length $l=6$, the $32$ fields comprise $8$ achiral fields and $24$ chiral fields forming $12$ mirror pairs. Uniform endogenous draws are racemic at the ensemble level, whereas ideal placement can select one member of a pair. A unique asymmetric terminal cap removes the candidate nonidentity stabilizers under the stated layer-preservation and realization conditions. The imported matched-source model yields an initiator surplus of $19.8$ units per period, exceeding the separate resource demands of $1$, $9$, or $18$ caps; saturated in-layer placement is available only on the compatible boundary columns, while other columns require external overhangs. Finally, a finite arm-sign model partitions the $D$ and $T$ states by stabilizer and gives an explicit orientation bias for fixed, identical anti or mixed states. Thermal restoration of blindness follows from invariance of the joint conformational measure under a single-partner half-turn. A correlated anti-state counterexample shows why symmetric one-unit marginals alone do not suffice. Exact enumeration, new verification code, and finite Lean certificates support the algebraic statements; the geometric and chemical interpretation is stated through explicit realization assumptions.

Annals of the Chrysene FormalismVol. 1(4)
Openalex Percentile: Top 27%
Chemistry and Stereochemistry Studies
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