scholarly journals Smart Organic Two-Dimensional Materials Based on a Rational Combination of Non-covalent Interactions

2016 ◽  
Vol 55 (36) ◽  
pp. 10707-10711 ◽  
Author(s):  
Wei Bai ◽  
Ziwen Jiang ◽  
Alexander E. Ribbe ◽  
S. Thayumanavan
Keyword(s):  
Two Dimensional ◽  
Two Dimensional Materials ◽  
Rational Combination ◽  
Non Covalent Interactions ◽  
Covalent Interactions

Smart Organic Two-Dimensional Materials Based on a Rational Combination of Non-covalent Interactions

2016 ◽  
Vol 128 (36) ◽  
pp. 10865-10869 ◽  
Author(s):  
Wei Bai ◽  
Ziwen Jiang ◽  
Alexander E. Ribbe ◽  
S. Thayumanavan
Keyword(s):  
Two Dimensional ◽  
Two Dimensional Materials ◽  
Rational Combination ◽  
Non Covalent Interactions ◽  
Covalent Interactions

scholarly journals Hybrid van der Waals heterojunction based on two-dimensional materials

2021 ◽  
Vol 2109 (1) ◽  
pp. 012012
Author(s):  
Cuicui Sun ◽  
Meili Qi
Keyword(s):  
2D Materials ◽  
Van Der Waals ◽  
Research Progress ◽  
Material Research ◽  
Two Dimensional ◽  
Covalent Bonds ◽  
2D Layered Materials ◽  
Two Dimensional Materials ◽  
Non Covalent Interactions ◽  
Heterostructure Devices

Abstract Since the discovery of graphene, two-dimensional (2D) layered materials have always been the focus of material research. The layers of 2D materials are covalent bonds, and the layers are weakly bonded to adjacent layers through van der Waals (vdW) interactions. Since any dangling-bond-free surface could be combined with another material through vdW forces, the concept can be extended. This can refer to the integration of 2D materials with any other non-2D materials through non-covalent interactions. The emerging mixed-dimensional (2D+nD, where n is 0, 1 or 3) heterostructure devices has been studied and represents a wider range of vdW heterostructures. New electronic devices and optoelectronic devices based on such heterojunctions have unique functions. Therefore, this article depicts the research progress of (2D+nD, where n is 0, 1 or 3) vdW heterojunctions based on 2D materials.

Multiple C-H⋯anion and N-H⋯anion Hydrogen Bond Directed Two-Dimensional Crystalline Nanosheet with Precise Distance Control of Surface Charges for Enhanced Capture DNA

Soft Matter ◽  
2021 ◽  
Author(s):  
Laicheng Zhou ◽  
Ran He ◽  
Yang Qin ◽  
Yi-Lin Wu ◽  
Li Jiang ◽  
...  
Keyword(s):  
Hydrogen Bond ◽  
Self Assembly ◽  
Two Dimensional ◽  
Surface Charges ◽  
Distance Control ◽  
Non Covalent Interactions ◽  
Covalent Interactions

Utilizing combined non-covalent interactions and introducing anions as structure-directing factors to build oriented self-assembly and 2D crystalline nanosheet superstructures with precise distance control of surface charges in competitive aqueous solvents...

Supramolecular 2D Monolayered Nanosheets Constructed by Using Synergy of Non-covalent Interactions

2021 ◽  
Author(s):  
Jing Zhang ◽  
Shuaiwei Qi ◽  
Chenyang Zhang ◽  
Wenzhe Wang ◽  
Qinwen Ding ◽  
...  
Keyword(s):  
Synergistic Effect ◽  
Noncovalent Interactions ◽  
Supramolecular Assemblies ◽  
Rational Approach ◽  
Two Dimensional ◽  
Non Covalent Interactions ◽  
Covalent Interactions

Here, a straightforward and rational approach to construct supramolecular assemblies with ordered nanostructure in a two-dimensional arrangement is reported. Taking advantage of the synergistic effect of multiple noncovalent interactions (hydrogen...

scholarly journals MOLECULAR FUNCTIONALIZATION OF 2D MATERIALS

2021 ◽  
pp. 2140002
Author(s):  
MIRIAM C. RODRÍGUEZ GONZÁLEZ ◽  
RAHUL SASIKUMAR ◽  
STEVEN DE FEYTER
Keyword(s):  
2D Materials ◽  
Layered Materials ◽  
Two Dimensional ◽  
Chemical Modifications ◽  
2D Layered Materials ◽  
Non Covalent Interactions ◽  
Covalent Interactions

In this paper, we give an overview of different chemical modifications that can be done on the surface of two-dimensional (2D) layered materials. We place emphasis on the diversity of reactions that have been proposed and are now available to surface scientists working in 2D materials field. Using mainly, but not exclusively, MoS2 as example, reactions involving covalent and non-covalent interactions are discussed.

NON COVALENT INTERACTIONS IN LARGE DIAMONDOID DIMERS IN THE GAS PHASE - A MICROWAVE STUDY

2017 ◽  
Author(s):  
Cristobal Perez ◽  
Melanie Schnell ◽  
Peter Schreiner ◽  
Norbert Mitzel ◽  
Yury Vishnevskiy ◽  
...  
Keyword(s):  
Gas Phase ◽  
Non Covalent Interactions ◽  
Covalent Interactions

Vapour Pressure Isotope Effect on Evaporation from Pure Organic Phases - a PIMD Approach

2020 ◽  
Author(s):  
Luis Vasquez ◽  
Agnieszka Dybala-Defratyka
Keyword(s):  
Path Integral ◽  
Vapour Pressure ◽  
Density Functional ◽  
Isotope Effects ◽  
Tight Binding ◽  
Decomposition Analysis ◽  
Energy Decomposition Analysis ◽  
Special Importance ◽  
Non Covalent Interactions ◽  
Covalent Interactions

<p></p><p>Very often in order to understand physical and chemical processes taking place among several phases fractionation of naturally abundant isotopes is monitored. Its measurement can be accompanied by theoretical determination to provide a more insightful interpretation of observed phenomena. Predictions are challenging due to the complexity of the effects involved in fractionation such as solvent effects and non-covalent interactions governing the behavior of the system which results in the necessity of using large models of those systems. This is sometimes a bottleneck and limits the theoretical description to only a few methods.<br> In this work vapour pressure isotope effects on evaporation from various organic solvents (ethanol, bromobenzene, dibromomethane, and trichloromethane) in the pure phase are estimated by combining force field or self-consistent charge density-functional tight-binding (SCC-DFTB) atomistic simulations with path integral principle. Furthermore, the recently developed Suzuki-Chin path integral is tested. In general, isotope effects are predicted qualitatively for most of the cases, however, the distinction between position-specific isotope effects observed for ethanol was only reproduced by SCC-DFTB, which indicates the importance of using non-harmonic bond approximations.<br> Energy decomposition analysis performed using the symmetry-adapted perturbation theory (SAPT) revealed sometimes quite substantial differences in interaction energy depending on whether the studied system was treated classically or quantum mechanically. Those observed differences might be the source of different magnitudes of isotope effects predicted using these two different levels of theory which is of special importance for the systems governed by non-covalent interactions.</p><br><p></p>

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