$\text{GSF-}\chi$: Global Stereochemical Fields for Chiral Graph Transformers

Understanding how chemical language models (CLMs) learn chemical meaning from molecular string representations, rather than only surface-level string patterns, is an important question in chemical representation learning and machine learning for chemistry. Chirality provides a demanding test case: enantiomers can differ greatly in pharmacological activity and toxicity, yet CLMs often struggle to distinguish chiral configurations reliably. Here we present Pan-CORE (Pan-Chemical Omniscale Representation Engine), a family of autoregressive Transformer-based encoder-decoder models for SMILES translation, and use high-temporal-resolution checkpoint analysis to investigate how chiral information is learned during training. Across all tested Pan-CORE variants, we observe a reproducible jump-up in which chiral-token accuracy rises abruptly after a long plateau, suggesting that chiral learning stagnation is not explained by model capacity alone and instead reflects the complexity of chiral constraints. Analyses of attention dynamics, residual-stream trajectories, and latent-space geometry support an encoder-centered mechanism in which chiral-token representations undergo transient destabilization and reconstruction, seen as a V-shaped drop and recovery in vector norm and directional stability, together with a clear reorganization of chiral molecular representations in the latent space. Encoder-decoder cross-evaluation further supports the encoder-centered nature of the transition, and targeted attention-head ablation identifies a small set of chiral-sensitive heads whose removal selectively reduces chiral-token accuracy even in the fully trained model. These findings show that SMILES translation can serve as a useful experimental system for mechanistic analysis of semantic emergence in CLMs, with implications for interpretable chemical representation learning.

Modern SMILES-based chemical language models obtain strong MoleculeNet performance by treating SMILES as generic text and compensating with multi-million-molecule self-supervised pretraining. We ask: when a domain carries structural priors as rich as chemistry's, does it warrant a domain-native transformer rather than a generic one rescued by scale? We answer affirmatively with \textbf{GM-Net} (Geometric Measure Network), a transformer family in which every module is replaced by a sphere-native counterpart, and instantiate it as \textbf{Chem-GMNet}. Three blocks follow: SH-Embedding (tokens as learnable directions on $S^{k-1}$ lifted through a Gegenbauer feature map); DualSKA (a per-head fusion of a linear-time gated Sphere-Flow recurrence whose persistent state we prove is the truncated multipole expansion of the input distribution, and a softmax Sphere-Kernel branch over the same Schoenberg-valid kernel); and SH-FFN (sphere projection $\to$ Gegenbauer lift $\to$ moment readout). On canonical DeepChem scaffold splits, against same-shape ChemBERTa-2 baselines under the chemberta3-faithful protocol: (i) random-initialised, Chem-GMNet wins on 7 of 10 MoleculeNet endpoints at $\sim\!35\%$ fewer parameters; (ii) pretrained on the same 10M-SMILES ZINC corpus as ChemBERTa-2 MLM-10M, it matches or beats the public release on 6 of 8 shared endpoints (5/7 excluding a known ClinTox release anomaly). A $(k,L)$ ablation shows that increasing the sphere dimension from $k\!=\!8$ to $k\!=\!10$ at fixed $L\!=\!3$ lowers ESOL RMSE to $0.938$ at scratch, beating pretrained ChemBERTa-2 MLM-10M on this endpoint without any pretraining at all.

Global self-attention drives modern graph transformers, yet the softmax at its core imposes a structural constraint rarely examined directly: every attention row is non-negative and sums to one, so each per-head output is a mass-conserving convex combination of value vectors. A node can never "attend to nothing." We argue this conservation constraint is a single root cause behind three pathologies usually studied in isolation: the collapse of node representations with depth (over-smoothing), a low-rank bottleneck on per-head outputs, and brittle optimization in deep stacks. Drawing on how sigmoid gating removes analogous attention sinks in language models, we introduce SigGate-GT, a graph transformer that applies a learned, per-head, input-conditioned sigmoid gate to the attention output inside the GraphGPS framework. The gate is a smooth, per-dimension "volume control" that can drive head outputs toward zero, relaxing the constraint without abandoning attention's probabilistic interpretation. Analytically and through synthetic experiments, we show the gate strictly increases the stable rank of per-head outputs, and connect this rank gain to all three manifestations. On five molecular and long-range benchmarks, SigGate-GT matches the prior best on ZINC (0.059 MAE), records the strongest result among the graph-transformer baselines we evaluate on ogbg-molhiv (82.47% ROC-AUC), and is competitive on ogbg-molpcba and the Long-Range Graph Benchmark, with statistically significant gains over GraphGPS on all five datasets (p < 0.05). Mechanism analyses confirm the diagnosis: gating slows over-smoothing (a 30% mean relative gain in representation diversity across 4-16 layers), keeps attention entropy from collapsing, and stabilizes training across a 10x learning-rate range, at about 1% parameter overhead on OGB and under 3% wall-clock cost.