arXiv subjects

Xueqian Kong

Publications and source records attributed to Xueqian Kong.

4 recordsLinked to original sources

arXiv2026

Multi-Agent Closed-Loop Reasoning for Organic Structure Elucidation from Multimodal Spectra

Following the molecular discovery and synthesis revolutions, scalable automated structure elucidation from routine spectroscopic data remains an outstanding challenge. Despite decades of computational efforts, no existing system achieved reliable reasoning over unseen spectra. Here, we propose MACROS, a multi-agent system automating structure elucidation by emulating expert iterative hypothesis-testing. Trained on 100M simulated and 1.6M experimental spectra-molecule pairs, it natively supports arbitrary combinations of routine spectroscopic techniques. It achieves unprecedented zero-shot generalization to diverse real-world samples, correctly identifying synthetic compounds, natural products and metabolites above 500 Da with 1D NMR. Remarkably, MACROS spontaneously recovers textbook spectroscopic correlations from unassigned data and exhibits emergent chemical intuition such as a ring-first parsing preference, learning fundamental chemical principles rather than memorizing database patterns. MACROS augments chemists via collaboration to deliver sixfold faster, 40% more accurate elucidation. MACROS establishes a scalable foundation for fully automated structure elucidation, and catalyzes accelerated molecular discovery toward autonomous laboratories.

physics.chem-ph↗

arXiv2026

Quantum Sensing with Triplet Pair States: A Theoretical Study

Molecular quantum sensors represent a promising frontier for the detection of nuclear magnetic resonance signals and alternating current magnetic fields at the nanoscale, potentially reaching single-proton sensitivity. Although the triplet states of molecular pentacene provide a viable sensing architecture, the triplet pair states produced by singlet fission of pentacene dimers could enable more flexible quantum manipulations through entanglement. In this work, we model the quantum sensing efficacy of a spin-polarized quintet manifold in a photoexcited pentacene dimer generated via intramolecular singlet fission. Using a Lindblad master equation approach, we simulate the evolution of the triplet pair state under standard dynamical decoupling sequences, including spin echo, XY4, and XY8 and provide a direct performance comparison to the traditional pentacene monomer benchmark. While both architectures exhibit comparable sensitivity for isolated single-spin detection, our findings indicate that the dimer architecture provides a superior interaction cross-section for detecting small ensembles of nuclear spins. Analytical expressions derived for fluorescence modulation demonstrate that sensitivity is optimized in the low-magnetic field regime and scales with the number of pulses in the sensing protocol. This study establishes a theoretical baseline for utilizing high-spin multi-excitonic states as chemically tunable, high-sensitivity quantum probes.

physics.chem-ph↗

arXiv2025

Triplet J-driven DNP, a proposal to increase the sensitivity of solution-state NMR without microwave

Dynamic nuclear polarization (DNP) is an important method to enhance the limited sensitivity of nuclear magnetic resonance (NMR). Using the existing mechanisms such as Overhauser DNP (ODNP) is still difficult to achieve significant enhancement of NMR signals in solutions at a high magnetic field. The recently proposed J-driven DNP (JDNP) condition (when the exchange interaction of two electron spins matches their Lamour frequency) may enable signal enhancement in solution as it requires only dipolar interaction between the biradical polarization agent and the analyte. However, likewise ODNP, the current JDNP strategy still requires the saturation of the electron polarization with high microwave power which has poor penetration and is associated with heating effects in most liquids. The replacement of high-power microwave irradiation is possible if the temporal electron polarization imbalance is created by a different wavelength such as the visible light. Here, we propose a triplet JDNP mechanism which first exploits the light-induced singlet fission process (i.e., a singlet exciton is converted into two triplet excitons). As the JDNP condition is fulfilled, a triplet-to-triplet cross-relaxation process will occur with different rates and consequently lead to the creation of hyperpolarization on the coupled nuclear spin states. This communication discusses the theory behind the triplet JDNP proposal, as well as the polarizing agents and conditions that will enable the new approach to enhance the sensitivity of NMR without the need of microwave irradiation.

physics.chem-ph↗

arXiv2022

A Unified Description for Polarization-Transfer Mechanisms in Magnetic Resonance in Static Solids: Cross Polarization and DNP

Polarization transfers are crucial building blocks in magnetic resonance experiments, i.e., they can be used to polarize insensitive nuclei and correlate nuclear spins in multidimensional NMR spectroscopy. The polarization can be transferred either across different nuclear spin species or from electron spins to the relatively low-polarized nuclear spins. The former route occurring in solid-state NMR (ssNMR) can be performed via cross polarization (CP), while the latter route is known as dynamic nuclear polarization (DNP). Despite having different operating conditions, we opinionate that both mechanisms are theoretically similar processes in ideal conditions, i.e., the electron is merely another spin-1/2 particle with a much higher gyromagnetic ratio. Here, we show that the CP and DNP processes can be described using a unified theory based on average Hamiltonian theory (AHT) combined with fictitious operators. The intuitive and unified approach has allowed new insights on the cross effect (CE) DNP mechanism, leading to better design of DNP polarizing agents and extending the applications beyond just hyperpolarization. We explore the possibility of exploiting theoretically predicted DNP transients for electron-nucleus distance measurements--like routine dipolar-recoupling experiments in solid-state NMR.

physics.chem-ph↗