Physical Chemistry Chemical Physics

doi: 10.1039/d3cp90092dpmid: N/A

doi: 10.1039/d3cp90093bpmid: N/A

Mengwen, Huang; Yasumura, Shinsaku; Toyao, Takashi; Shimizu, Ken-ichi; Maeno, Zen

doi: 10.1039/d3cp00478cpmid: 36988320

Metal-exchanged zeolites have great potential to form unique active metal species and develop their catalysis by promoting small molecules such as light alkanes. Ga-exchanged zeolites have attracted attention as promising heterogeneous catalysts for dehydrogenative light-alkane transformations. The speciation of active Ga species in reduced and oxidized Ga-exchanged zeolites and their reaction mechanisms have been discussed in several studies based on experimental and theoretical investigations. In contrast, studies on In-exchanged zeolites have been far less explored, and thus active In-species have rarely been investigated. In this perspective, we summarized our investigations on In- and Ga-exchanged zeolites for light-alkane transformations. Our research group reported the formation of In–oxo clusters using the O2 treatment of In-CHA and their potential for the partial oxidation of CH4 (POM) at room temperature. We also observed the formation of In-hydrides in CHA zeolites during the preparation through reductive solid-state ion-exchange (RSSIE) and revealed their catalysis for non-oxidative C2H6 dehydrogenation (EDH). Their detailed structures and reaction mechanisms are discussed in combination with spectroscopic, kinetic, and theoretical studies. Furthermore, comparative studies on the formation of Ga-oxo clusters for POM at room temperature and the controlled formation of Ga-hydrides for selective EDH were conducted. The obtained results and insights are comprehensively discussed, including the relationship between the local structure of the active In/Ga species and reaction selectivity, as well as the influence of different zeolite frameworks on the formation of active species.

Martín Pendás, Ángel; Francisco, Evelio; Suárez, Dimas; Costales, Aurora; Díaz, Natalia; Munárriz, Julen; Rocha-Rinza, Tomás; Guevara-Vela, José Manuel

doi: 10.1039/d2cp05540fpmid: 36994471

In this perspective, we review some recent advances in the concept of atoms-in-molecules from a real space perspective. We first introduce the general formalism of atomic weight factors that allows unifying the treatment of fuzzy and non-fuzzy decompositions under a common algebraic umbrella. We then show how the use of reduced density matrices and their cumulants allows partitioning any quantum mechanical observable into atomic or group contributions. This circumstance provides access to electron counting as well as energy partitioning, on the same footing. We focus on how the fluctuations of atomic populations, as measured by the statistical cumulants of the electron distribution functions, are related to general multi-center bonding descriptors. Then we turn our attention to the interacting quantum atom energy partitioning, which is briefly reviewed since several general accounts on it have already appeared in the literature. More attention is paid to recent applications to large systems. Finally, we consider how a common formalism to extract electron counts and energies can be used to establish an algebraic justification for the extensively used bond order–bond energy relationships. We also briefly review a path to recover one-electron functions from real space partitions. Although most of the applications considered will be restricted to real space atoms taken from the quantum theory of atoms in molecules, arguably the most successful of all the atomic partitions devised so far, all the take-home messages from this perspective are generalizable to any real space decompositions.

Rodrigues, Ana Clara B.; Lopes, Susana M. M.; Cunha, Carla; Braz, João; Pinho e Melo, Teresa M. V. D.; Seixas de Melo, J. Sérgio; Pineiro, Marta

doi: 10.1039/d2cp05941jpmid: 36919842

A comprehensive study on the electronic spectral, photophysical and acid–base properties of phenyl- and methyl-oxime corrole derivatives and of triphenylcorrole (model corrole) has been performed, aiming to shed light on the existing species in the ground and excited states. Solvents and corrole concentration are found to govern the properties of the studied compounds and are determinants of their applicability in in vivo studies. In THF, the neutral corrole has two tautomeric forms (T1 and T2). In DMSO, the deprotonated form shows a characteristic long-wavelength Q band slightly shifted to blue when compared with the T1 tautomer and a higher fluorescence quantum yield. In ACN, with the increase of the corrole concentration formation of an aggregate due to homoconjugation (with dimer characteristics) is observed, and pioneeringly reported using UV-Vis and fluorescence studies and confirmed by carrying out titrations with TFA. The effect of the oxime group on the pK values of a corrole is found to influence the formation of a homoconjugate, namely by precluding its formation (at higher concentrations) when compared with the model corrole. TDDFT electronic quantum calculations support the experimental observations, namely the existence of tautomers and deprotonated species, with their respective electronic spectral features, further allowed proposing a structure for the homoconjugate complex in ACN. The characteristics of the oxime-corroles, namely a pK of ∼ 5, absorption and emission at ca. 650 nm and solvent dependent properties, make them good candidates for their use in biological systems either as probes, sensors, or as new sensitizers for photodynamic therapy.

Zhu, Hongjuan; Zhang, Danyang; Feng, Eryin; Sheng, Xiaowei

doi: 10.1039/d2cp04372fpmid: 36883359

In the present paper, the aggregated structures of zinc phthalocyanine (ZnPc) have been investigated by considering its dimers and trimers. Based on the density functional theory calculations, two stable conformations are obtained for the ZnPc dimer and trimer, respectively. The IGMH (independent gradient model based on the Hirshfeld partition of molecular density) analysis reveals that the π–π interaction between the ZnPc molecules causes the aggregation. Normally, stacked structures with a slight displacement are favorable for aggregation. In addition, the planar structure of the ZnPc monomer is largely maintained in the aggregated conformations. For the presently obtained structures, the first singlet excited state absorption (ESA) spectra of these aggregated conformations of ZnPc were calculated based on the linear-response time-dependent density functional theory (LR-TDDFT), which has been well applied by our group. The results of the excited state absorption spectra reveal that the aggregation causes the ESA band to blue shift compared to the ZnPc monomer. By using the conventional description of the interaction between monomer transition dipoles, this blue shift is elucidated by the side-by-side transition dipole moments in the constituted monomers. The present results for the ESA combined with the previously reported results for ground state absorption (GSA) will provide guidelines to tune the window of the optical-limiting effect for the ZnPc based materials.

Specht, Thomas; Münnemann, Kerstin; Hasse, Hans; Jirasek, Fabian

doi: 10.1039/d3cp00509gpmid: 36987633

Poorly specified mixtures, whose composition is unknown, are ubiquitous in chemical and biochemical engineering. In the present work, we propose a rational method for defining and quantifying pseudo-components in such mixtures that is free of ad hoc assumptions. The new method requires only standard nuclear magnetic resonance (NMR) experiments and can be fully automated. In the first step, the method analyzes the composition of the poorly specified mixture in terms of structural groups, which is much easier than obtaining the component speciation. The structural groups are then clustered into pseudo-components based on information on the self-diffusion coefficients measured by pulsed-field gradient (PFG) NMR spectroscopy. We demonstrate the performance of the new method on several aqueous mixtures. The method is broadly applicable and provides a sound basis for modeling and simulation of processes with poorly specified mixtures, without the need for tedious and expensive structure elucidation. It is also attractive for process monitoring.

Zhang, Lei; Yu, Yuanxi; Suo, Liumin; Zhuang, Wei; He, Lunhua; Zhang, Xiaohua; Hong, Liang; Tan, Pan

doi: 10.1039/d3cp00803gpmid: 36987745

Water-in-salt electrolytes (WiSEs) have attracted extensive attention as promising alternatives to organic electrolytes. The limited electrochemical stability windows (ESWs) of aqueous electrolytes are significantly widened by WiSEs. However, the actual ESWs are lower than predicted as the interphase with WiSEs is not as stable as the solid electrolyte interphase (SEI) in conventional lithium-ion batteries. Therefore, identifying the interface state in WiSEs is vital to understanding their electrochemical behavior. Here, the structure of the lithium bis(trifluoromethane sulfonyl)imide (LiTFSI) electrolyte near the interface of the carbon electrode (Ketjen black) was evaluated by experimental methods (neutron diffraction, Raman, and nuclear magnetic resonance spectroscopy) and molecular dynamics (MD) simulations. The results reveal that the introduction of carbon electrodes increases the size of the anionic nanoclusters and enhances the microphase separation at the interface. The MD simulations show that cation–π interactions are responsible for the evolution of anionic nanoclusters at the electrode interface. Moreover, lower charge transfer resistance is achieved at carbon-based electrodes due to the specific interface state. Our findings provide a strategy for introducing cation–π interactions between electrodes and electrolytes to improve the electrochemical performance.

Li, Hui-Yuan; Qin, Gui-Ya; Lin, Pan-Pan; Sun, Xiao-Qi; Fan, Jian-Xun; Wang, Rui; Li, Hui; Zou, Lu-Yi; Guo, Jing-Fu; Ren, Ai-Min

doi: 10.1039/d3cp00567dpmid: 36987913

To date, the manipulation of intermolecular nonconjugation interactions in organic crystals is still a great challenge due to the complexity of weak intermolecular interactions. Here we designed molecules substituted by β-methylselenyl on naphtho[1,2-b:5,6-b′]dithiophene and anthra[2,3-b:6,7-b′]dithiophene, respectively (anti-β-MS-NDT, anti-β-MS-ADT), which together with anti-β-MS-BDT synthesized experimentally all exhibited 2D brickwork π-stacking. Moreover, their maximum molecular carrier mobilities reached 3.30 and 16.46 cm2 V−1 s−1. These results indicated that the substitution of β-methylselenyl could be a strategy to directionally adjust the parent herringbone stacking into 2D brickwork π-stacking. Hirshfeld surface analysis and symmetry-adapted perturbation theory (SAPT) were used to investigate the nonconjugated interactions in the pitched π-stacking formed by the β-methylthio-substituted acenedithiophene derivatives and the 2D brickwork π-stacking of the β-methylselenyl-substituted ones; wherein, the steric hindrance caused by the introduction of the substituents promoted Csp2–Csp2⋯π interactions to replace Csp2–H⋯π to stabilize the face-to-face stacking. Moreover, by calculating the decomposition energy of the intermediate state model of the molecular stacking mode that may exist in the replacement conversion process, it was found that the energy of this intermediate state was larger than that of the actual ones, finally confirming the inevitability of the actual existence in this stacking. In addition, because of the reduction in intensity of the special vibration modes, it could be found that the β-methylselenyl substitution showed better phonon assistance than β-methylthio substitution in terms of dynamic disorder. This study is a further step toward fully understanding the relationship between intermolecular interactions and regulation of the molecular stacking.

Hernández Velázquez, J. D.; Sánchez-Balderas, G.; Gama Goicochea, A.; Pérez, E.

doi: 10.1039/d2cp04321apmid: 36987944

The effective solid–liquid interfacial tension (SL-IFT) between pure liquids and rough solid surfaces is studied through coarse-grained simulations. Using the dissipative particle dynamics method, we design solid–liquid interfaces, confining a pure liquid between two explicit solid surfaces with different roughness degrees. The roughness of the solid phase is characterized by Wenzel's roughness factor and the effective SL-IFT is reported as a function of it also. Two solid–liquid systems, different from each other by their solid–liquid repulsion strength, are studied to measure the effects caused by the surface roughness on the calculation of . It is found that the roughness changes the structure of the liquid, which is observed in the first layer of liquid near the solid. These changes are responsible for the effective SL-IFT increase, as surface roughness increases. Although there is a predominance of surface roughness in the calculation of it is found that the effective SL-IFT is directly proportional to the magnitude of the solid–liquid repulsion strength. The insights provided by these simulations suggest that the increase of Wenzel's roughness factor increases the number of effective solid–liquid interactions between particles, yielding significant changes in the local values of the normal and tangential components of the pressure tensor.