Langstonmcculloch6799

Density functional theory (DFT) calculations on the m-CPBA adduct complexes show that the ligand-field-splitting energy increases with an increase of the ring size of the diamine moiety, as in the case of the starting copper(II) complexes, which enhances the reactivity of the m-CPBA adduct complexes. The reasons for such different reactivities of the m-CPBA adduct complexes are evaluated by using DFT calculations.The efficient implementation of the TWOE program for evaluating the atomic and interatomic energy components at post-HF level was developed. The systematic convergence of these terms up to a near full-CI limit was performed for the first time for a series of coupled cluster methods CCSD → CCSDT → CCSDTQ → CCSDTQP. A comparison with corresponding CI approaches (up to fifth excitation level) is additionally discussed. For a set of diatomic systems, it was demonstrated that, along with a full molecular energy convergence, all its components are also converged but with different patterns. It was found that not all components are decreased in their values at increasing computational rank. For instance, atomic energy parts are decreased while interatomic (interaction) energies are increased as the limiting level is approached. Two schemes were employed for atomic partition of molecules the Baders approach and planes dissection. Influence of dynamical correlation effects on atomic energy components was analyzed in detail. Current TWOE implementation allows one, in principle, to work with any ab initio method providing the two-particle density matrix. It is believed that the developed program will be a useful tool for a real space energy decomposition that helps to reveal the most peculiar points in the structure of the total and correlation energies of a molecule.The end-capping group (EG) is the essential electron-withdrawing component of nonfullerene acceptors (NFAs) in bulk heterojunction (BHJ) organic solar cells (OSCs). To systematically probe the impact of two frequent EG functionalization strategies, π-extension and halogenation, in A-DAD-A type NFAs, we synthesized and characterized four such NFAs BT-BIC, LIC, L4F, and BO-L4F. To assess the relative importance of these strategies, we contrast these NFAs with the baseline acceptors, Y5 and Y6. Up to 16.6% power conversion efficiency (PCE) in binary inverted OSCs with BT-BO-L4F combining π-extension and halogenation was achieved. When these two factors are combined, the effect on optical absorption is cumulative. Single-crystal π-π stacking distances are similar for the EG strategies of π-extension. Increasing the alkyl substituent length from BT-L4F to BT-BO-L4F significantly alters the packing motif and eliminates the EG core interactions of BT-L4F. Electronic structure computations reveal some of the largest NFA π-π electronic couplings observed to date, 103.8 meV in BT-L4F and 47.5 meV in BT-BO-L4F. Computed electronic reorganization energies, 132 and 133 meV for BT-L4F and BT-BO-L4F, respectively, are also lower than Y6 (150 meV). BHJ blends show preferential π-face-on orientation, and both fluorination and π-extension increase NFA crystallinity. selleck compound Femto/nanosecond transient absorption spectroscopy (fs/nsTA) and integrated photocurrent device analysis (IPDA) indicate that π-extension modifies the phase separation to enhance film ordering and carrier mobility, while fluorination suppresses unimolecular recombination. This systematic study highlights the synergistic effects of NFA π-extension and fluorination in affording efficient OSCs and provides insights into designing next-generation materials.Understanding the finely orchestrated interactions leading to or preventing programmed cell death (apoptosis) is of utmost importance in cancer research because the failure of these systems could eventually lead to the onset of the disease. In this regard, the maintenance of a delicate balance between the promoters and inhibitors of mitochondrial apoptosis is crucial, as demonstrated by the interplay among the Bcl-2 family members. In particular, B-cell lymphoma extra-large (Bcl-xL) is a target of interest due to the forefront role of its dysfunctions in cancer development. Bcl-xL prevents apoptosis by binding both the pro-apoptotic BH3-only proteins, like PUMA, and the noncanonical partners, such as p53, at different sites. An allosteric communication between the BH3-only protein binding pocket and the p53 binding site, mediating the release of p53 from Bcl-xL upon PUMA binding, has been postulated and supported by nuclear magnetic resonance and other biophysical data. The molecular details of this mechanism, especially at the residue level, remain unclear. In this work, we investigated the distal communication between these two sites in Bcl-xL in its free state and when bound to PUMA. We also evaluated how missense mutations of Bcl-xL found in cancer samples might impair this communication and therefore the allosteric mechanism. We employed all-atom explicit solvent microsecond molecular dynamics simulations, analyzed through a Protein Structure Network approach and integrated with calculations of changes in free energies upon cancer-related mutations identified by genomics studies. We found a subset of candidate residues responsible for both maintaining protein stability and for conveying structural information between the two binding sites and hypothesized possible communication routes between specific residues at both sites.Integrated optics shows great potential in the current optical communication systems, sensor technology, optical computers, and other fields. Tunable laser technology within a certain range is the key to achieving on-chip optical integration; to realize which, Raman scattering is a competitive method that can effectively transfer incident laser energy to optical phonons due to the photon-phonon interaction. Here, we take hexagonal boron nitride as the energy conversion medium, and based on the angle-resolved polarized Raman spectroscopy, it is found that when laser polarization vector ei ⊥ c axis, the spectrum obtains maximal scattering across the cross section and a minimal depolarization ratio. At room temperature, h-BN obtains an output signal with a wavelength of 522.8 nm and a full-width at half-maximum of 0.24 nm under the excitation of 488 nm pump laser, and the depolarization ratio is 0.09 (theoretically, it is 0, and this difference is due to experimental errors). And then, within the temperature range of 80∼420 K, the scattered light wavelength shows a high-precision shift of 0.