2 research outputs found
Bioactive Azaphilone Derivatives from the Fungus <i>Talaromyces aculeatus</i>
Six new azaphilone derivatives, talaraculones
A–F (<b>1</b>–<b>6</b>), together with five
known analogues (<b>7</b>–<b>11</b>), were obtained
from the saline soil-derived fungus <i>Talaromyces aculeatus</i>. The absolute configurations of <b>1</b> and <b>6</b> were assigned by quantum chemical calculations of the electronic
circular dichroism (ECD) spectra. Compounds <b>1</b> and <b>5</b> represent the first reported azaphilone derivatives with
a C4 aliphatic side chain and a methylal group at C-3, respectively.
Talaraculones A and B (<b>1</b> and <b>2</b>) exhibited
stronger inhibitory activity against α-glucosidase than the
positive control acarbose (IC<sub>50</sub> = 101.5 μM), with
IC<sub>50</sub> values of 78.6 and 22.9 μM, respectively
Phonon Resonance Catalysis in NO Oxidation on Mn-Based Mullite
A phonon is the medium a bulk material used to exchange
energy
with the environment and is thus crucial for heterogeneous catalysis.
However, a physical correlation between phonons and catalytic processes
has not been established yet. Herein, by combining various in situ
characterization techniques, we discovered the intrinsic correlations
between phonon modes and the vibrations of reactant intermediates
during NO oxidation on the mullite catalyst YMn2O5. It was found that the active phonon modes (350 (Ag(5))
and 670 cm–1 (B1g(12))) are strongly
correlated with the vibrational frequencies of the adsorbed −O2 and −O–NO2 intermediates. The resulting
resonance will transfer the superposed energy (nℏω) of the high-energy phonons to reactants one by one via the unit
energy (ℏω) and then increase the vibrational
amplitude along the reaction direction, contributing to the increase
in the entropy of the surface reactants and thus the reduction of
the Gibbs energy of activation. Phonon resonance catalysis (PRCAT)
was thus proposed based on this discovery. This work provides insights
into the bidirectional selection of catalysts and precise chemical
reactions by matching catalyst phonons with reactant vibrational frequencies