Relevant bibliographies by topics / Intermolecular interactions

Academic literature on the topic 'Intermolecular interactions'

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Published: 4 June 2021
Last updated: 8 June 2024

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Journal articles on the topic "Intermolecular interactions"

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Klemperer, W. "Intermolecular Interactions." Science 257, no. 5072 (August 14, 1992): 887–88. http://dx.doi.org/10.1126/science.257.5072.887.

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Tolipov, I. A., and M. P. Kholmurodov. "TYPES OF INTERMOLECULAR INTERACTIONS AND THEIR MODERN PHYSICAL SIGNIFICANCE." American Journal of Applied Science and Technology 4, no. 4 (April 1, 2024): 15–23. http://dx.doi.org/10.37547/ajast/volume04issue04-04.

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This article examines the important factors of intermolecular interactions to study the basic properties and physical nature of substances. Various optical methods have been used to study the nature and mechanism of intermolecular interactions. The properties of substances are revealed in detail, what molecules it consists of and how these molecules are located in relation to each other.
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Kumar Panja, Sumit. "Weak Intermolecular Interactions and Molecular Cluster in Ionic Liquids." Oriental Journal of Physical Sciences 6, no. 1-2 (February 28, 2022): 04–06. http://dx.doi.org/10.13005/ojps06.01-02.02.

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Presently, we are working on weak intermolecular interaction (aliphatic H-bonding and ?-? stacking interaction) in imidazolium and piperidinium-based ionic liquids. The weak interactions play a crucial role in the physical properties of ILs. Further, the significance of weak interactions on cluster formation and extended intermolecular interaction in these ILs have been investigated in our laboratory. The vibrational spectroscopic techniques (Raman and FTIR) have been employed to understand the effect of H-bonding interaction on physical property and molecular cluster formation of ILs. Further, DFT calculations help for better understanding the intermolecular interactions at the molecular level.
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Ren, Hai-Chao, Lin-Xiang Ji, Tu-Nan Chen, Xian-Zhen Jia, Rui-Peng Liu, Xiu-Qing Zhang, Dong-Qing Wei, Xiao-Feng Wang, and Guang-Fu Ji. "Intermolecular Vibration Energy Transfer Process in Two CL-20-Based Cocrystals Theoretically Revealed by Two-Dimensional Infrared Spectra." Molecules 27, no. 7 (March 26, 2022): 2153. http://dx.doi.org/10.3390/molecules27072153.

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Inspired by the recent cocrystallization and theory of energetic materials, we theoretically investigated the intermolecular vibrational energy transfer process and the non-covalent intermolecular interactions between explosive compounds. The intermolecular interactions between 2,4,6-trinitrotoluene (TNT) and 2,4,6,8,10,12-hexanitro-2,4,6,8,10,12-hexaazaisowurtzitane (CL-20) and between 1,3,5,7-tetranitro-1,3,5,7-tetrazocane (HMX) and CL-20 were studied using calculated two-dimensional infrared (2D IR) spectra and the independent gradient model based on the Hirshfeld partition (IGMH) method, respectively. Based on the comparison of the theoretical infrared spectra and optimized geometries with experimental results, the theoretical models can effectively reproduce the experimental geometries. By analyzing cross-peaks in the 2D IR spectra of TNT/CL-20, the intermolecular vibrational energy transfer process between TNT and CL-20 was calculated, and the conclusion was made that the vibrational energy transfer process between CL-20 and TNTII (TNTIII) is relatively slower than between CL-20 and TNTI. As the vibration energy transfer is the bridge of the intermolecular interactions, the weak intermolecular interactions were visualized using the IGMH method, and the results demonstrate that the intermolecular non-covalent interactions of TNT/CL-20 include van der Waals (vdW) interactions and hydrogen bonds, while the intermolecular non-covalent interactions of HMX/CL-20 are mainly comprised of vdW interactions. Further, we determined that the intermolecular interaction can stabilize the trigger bond in TNT/CL-20 and HMX/CL-20 based on Mayer bond order density, and stronger intermolecular interactions generally indicate lower impact sensitivity of energetic materials. We believe that the results obtained in this work are important for a better understanding of the cocrystal mechanism and its application in the field of energetic materials.
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Wójcik, Marek J. "Intermolecular interactions in water." Journal of Molecular Structure 189, no. 1-2 (October 1988): 89–103. http://dx.doi.org/10.1016/0022-2860(88)80215-1.

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Reisse, J., M. Claessens, O. Fabre, G. Michaux, M. L. Stien, and D. Zimmermann. "Heterocycles and Intermolecular Interactions." Bulletin des Sociétés Chimiques Belges 92, no. 9 (September 1, 2010): 819–24. http://dx.doi.org/10.1002/bscb.19830920908.

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Alhameedi, Khidhir, Amir Karton, Dylan Jayatilaka, and Sajesh P. Thomas. "Bond orders for intermolecular interactions in crystals: charge transfer, ionicity and the effect on intramolecular bonds." IUCrJ 5, no. 5 (August 29, 2018): 635–46. http://dx.doi.org/10.1107/s2052252518010758.

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The question of whether intermolecular interactions in crystals originate from localized atom...atom interactions or as a result of holistic molecule...molecule close packing is a matter of continuing debate. In this context, the newly introduced Roby–Gould bond indices are reported for intermolecular `σ-hole' interactions, such as halogen bonding and chalcogen bonding, and compared with those for hydrogen bonds. A series of 97 crystal systems exhibiting these interaction motifs obtained from the Cambridge Structural Database (CSD) has been analysed. In contrast with conventional bond-order estimations, the new method separately estimates the ionic and covalent bond indices for atom...atom and molecule...molecule bond orders, which shed light on the nature of these interactions. A consistent trend in charge transfer from halogen/chalcogen bond-acceptor to bond-donor groups has been found in these intermolecular interaction regionsviaHirshfeld atomic partitioning of the electron populations. These results, along with the `conservation of bond orders' tested in the interaction regions, establish the significant role of localized atom...atom interactions in the formation of these intermolecular binding motifs.
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Lovelock, Kevin R. J. "Quantifying intermolecular interactions of ionic liquids using cohesive energy densities." Royal Society Open Science 4, no. 12 (December 2017): 171223. http://dx.doi.org/10.1098/rsos.171223.

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For ionic liquids (ILs), both the large number of possible cation + anion combinations and their ionic nature provide a unique challenge for understanding intermolecular interactions. Cohesive energy density, ced , is used to quantify the strength of intermolecular interactions for molecular liquids, and is determined using the enthalpy of vaporization. A critical analysis of the experimental challenges and data to obtain ced for ILs is provided. For ILs there are two methods to judge the strength of intermolecular interactions, due to the presence of multiple constituents in the vapour phase of ILs. Firstly, ced IP , where the ionic vapour constituent is neutral ion pairs, the major constituent of the IL vapour. Secondly, ced C+A , where the ionic vapour constituents are isolated ions. A ced IP dataset is presented for 64 ILs. For the first time an experimental ced C+A , a measure of the strength of the total intermolecular interaction for an IL, is presented. ced C+A is significantly larger for ILs than ced for most molecular liquids, reflecting the need to break all of the relatively strong electrostatic interactions present in ILs. However, the van der Waals interactions contribute significantly to IL volatility due to the very strong electrostatic interaction in the neutral ion pair ionic vapour. An excellent linear correlation is found between ced IP and the inverse of the molecular volume. A good linear correlation is found between IL ced IP and IL Gordon parameter (which are dependent primarily on surface tension). ced values obtained through indirect methods gave similar magnitude values to ced IP . These findings show that ced IP is very important for understanding IL intermolecular interactions, in spite of ced IP not being a measure of the total intermolecular interactions of an IL. In the outlook section, remaining challenges for understanding IL intermolecular interactions are outlined.
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Jakubec, Martin, Ivana Císařová, Jindřich Karban, and Jan Sýkora. "The Effect of Deoxyfluorination on Intermolecular Interactions in the Crystal Structures of 1,6-Anhydro-2,3-epimino-hexopyranoses." Molecules 27, no. 1 (January 3, 2022): 278. http://dx.doi.org/10.3390/molecules27010278.

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The effect of substitution on intermolecular interactions was investigated in a series of 1,6-anhydro-2,3-epimino-hexopyranoses. The study focused on the qualitative evaluation of intermolecular interactions using DFT calculations and the comparison of molecular arrangements in the crystal lattice. Altogether, ten crystal structures were compared, including two structures of C4-deoxygenated, four C4-deoxyfluorinated and four parent epimino pyranoses. It was found that the substitution of the original hydroxy group by hydrogen or fluorine leads to a weakening of the intermolecular interaction by approximately 4 kcal/mol. The strength of the intermolecular interactions was found to be in the following descending order: hydrogen bonding of hydroxy groups, hydrogen bonding of the amino group, interactions with fluorine and weak electrostatic interactions. The intermolecular interactions that involved fluorine atom were rather weak; however, they were often supported by other weak interactions. The fluorine atom was not able to substitute the role of the hydroxy group in molecular packing and the fluorine atoms interacted only weakly with the hydrogen atoms located at electropositive regions of the carbohydrate molecules. However, the fluorine interaction was not restricted to a single molecule but was spread over at least three other molecules. This feature is a base for similar molecule arrangements in the structures of related compounds, as we found for the C4-Fax and C4-Feq epimines presented here.
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Srinivasan, Mythily, and A. Keith Dunker. "Proline Rich Motifs as Drug Targets in Immune Mediated Disorders." International Journal of Peptides 2012 (May 16, 2012): 1–14. http://dx.doi.org/10.1155/2012/634769.

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The current version of the human immunome network consists of nearly 1400 interactions involving approximately 600 proteins. Intermolecular interactions mediated by proline-rich motifs (PRMs) are observed in many facets of the immune response. The proline-rich regions are known to preferentially adopt a polyproline type II helical conformation, an extended structure that facilitates transient intermolecular interactions such as signal transduction, antigen recognition, cell-cell communication and cytoskeletal organization. The propensity of both the side chain and the backbone carbonyls of the polyproline type II helix to participate in the interface interaction makes it an excellent recognition motif. An advantage of such distinct chemical features is that the interactions can be discriminatory even in the absence of high affinities. Indeed, the immune response is mediated by well-orchestrated low-affinity short-duration intermolecular interactions. The proline-rich regions are predominantly localized in the solvent-exposed regions such as the loops, intrinsically disordered regions, or between domains that constitute the intermolecular interface. Peptide mimics of the PRM have been suggested as potential antagonists of intermolecular interactions. In this paper, we discuss novel PRM-mediated interactions in the human immunome that potentially serve as attractive targets for immunomodulation and drug development for inflammatory and autoimmune pathologies.
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Dissertations / Theses on the topic "Intermolecular interactions"

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Randall, Karen L. "Studies of intermolecular interactions." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1997. http://www.collectionscanada.ca/obj/s4/f2/dsk2/tape16/PQDD_0014/NQ28043.pdf.

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Hurst, G. J. B. "Intermolecular interactions by perturbation theory." Thesis, University of Cambridge, 1985. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.356653.

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Clark, Jane Northen. "Intermolecular interactions in polymer blends." Thesis, Imperial College London, 1990. http://hdl.handle.net/10044/1/47811.

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Varley, Lisa. "Intermolecular interactions : quantification and applications." Thesis, University of Sheffield, 2012. http://etheses.whiterose.ac.uk/2739/.

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This thesis deals with the nature of fundamental intermolecular interactions and the ways in which they can be exploited using supramolecular chemistry. Three separate studies have been undertaken in order to explore and quantify different types of electrostatic interactions. Chapter 2 describes an investigation into the nature of hydrogen bonding interactions between charged species and well-defined neutral hosts, in order to quantify their hydrogen bonding strength on an already established scale. The importance of metal-ligand interactions in self-assembly is documented in Chapter 3, where the synthesis of functional supramolecules is described and their self-assembly in the presence of a bidentate ligand is investigated. Finally, Chapter 4 describes the use of calixarene-porphyrin conjugates in gas-sensing devices, showing how a handle on the design and synthesis of supramolecules and an understanding of their basic interactions can provide a useful application. The detailed background literature relating to the project will be described as an introduction to each chapter; this chapter provides a general introduction to the field of supramolecular chemistry and an overview of key advances that have been made since its inception.
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Moujaes, Elie A. "Intermolecular vibronic interactions in fullerene anions." Thesis, University of Nottingham, 2007. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.438359.

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Hudson, Amanda Gayle. "Characterization of Intermolecular Interactions in Nanostructured Materials." Diss., Virginia Tech, 2015. http://hdl.handle.net/10919/77855.

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Advanced analytical techniques were utilized to investigate the intermolecular forces in several nanostructured materials. Techniques including, but not limited to, isothermal titration calorimetry (ITC), variable temperature Fourier transform infrared (FTIR) spectroscopy, and ultraviolet-visible (UV-Vis) thermal curves were used to study the fundamental interactions present in various nanomaterials, and to further probe the influence of these interactions on the overall behavior of the material. The areas of focus included self-assembly of surfactant micelles, polycation complexation of DNA, and temperature-dependent hydrogen bonding in polymeric systems. ITC was successfully used to determine the low critical micelle concentration (CMC) for a novel gemini surfactant with limited water solubility. CMCs were measured at decreasing methanol molar fractions (xMeOH) in water and the resulting linear relationship between CMC and methanol concentration was used to mathematically extrapolate to a predicted CMC at xMeOH = 0. Using this technique, the CMC value for the novel gemini surfactant was predicted to be 0.037 ± 0.004 mM. This extrapolation technique was also validated with surfactant standards. ITC was also used to investigate the binding thermodynamics of polyplex formation with polycations and DNA. The imidazolium-containing and trehalose-based polycations were both found to have endothermic, entropically driven binding with DNA, while the adenine-containing polycation exhibited exothermic DNA binding. In addition, ITC was also used to confirm the stoichiometric binding ratio of linear polyethylenimine and DNA polyplexes as determined by a novel NMR method. Dynamic light scattering (DLS) and zeta potential measurements were also performed to determine the size and surface charge of polyplexes. Circular dichroism (CD) and FTIR spectroscopies provided information regarding the structural changes that may occur in the DNA upon complexation with polymers. UV-Vis thermal curves indicated that polyplexes exhibit a greater thermal stability than DNA by itself. Variable temperature FTIR spectroscopy was used to quantitatively compare the hydrogen bonding behavior of multi-walled carbon nanotube (MWCNT)-polyurethane composites. Spectra were collected from 35 to 185 deg C for samples containing various weight percent loadings of MWCNTs with different hydrogen bonding surface functionalities. Peak fitting analysis was performed in the carbonyl-stretching region for each sample, and the hydrogen-bonding index (Rindex) was reported. Rindex values were used to quantitatively compare all of the composite samples in regards to temperature effects, weight percent loadings of MWCNTs, and the different functionalizations. In general, higher weight percent loadings of the MWCNTs resulted in greater Rindex values and increased hydrogen bond dissociation temperatures. In addition, at 5 and 10 wt% loadings the initial Rindex values displayed a trend that tracked well with the increasing hydrogen bonding capacity of the various surface functionalities.
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Inglefield, Jr David Lott. "Tailoring Intermolecular Interactions for High-Performance Nanocomposites." Diss., Virginia Tech, 2001. http://hdl.handle.net/10919/64411.

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Acid oxidation of multi-walled carbon nanotubes (MWCNTs) introduced carboxylic acid sites onto the MWCNT surface, which permitted further functionalization. Derivatization of carboxylic acid sites yielded amide-amine and amide-urea functionalized MWCNTs from oxidized precursors. Conventional MWCNT characterization techniques including X-ray photoelectron spectroscopy (XPS), thermogravimetric analysis (TGA), and Raman spectroscopy supported successful MWCNT functionalization. Incorporation of MWCNTs functionalized with hydrogen bonding groups into a segmented polyurethane matrix led to an increase in mechanical properties at optimized MWCNT loadings, in contrast with non-functionalized MWCNTs that resulted in mechanical property decreases across all loadings. Dynamic mechanical analysis (DMA) demonstrated an increase in the polyurethane-MWCNT composite flow temperature with increasing hydrogen bonding MWCNT incorporation, as opposed to non-functionalized MWCNT composites which displayed no significant change in flow temperature. Variable temperature Fourier transform infrared spectroscopy (VT FT-IR) probed temperature-dependent hydrogen bonding in the polyurethane-MWCNT composites and revealed a significant impact on composite hydrogen bonding interactions upon MWCNT incorporation, which was amplified in composites formed using hydrogen bonding functionalized MWCNTs. Acid oxidation of carbon nanohorns (CNHs) yielded carboxylic acid functionalized CNHs, providing sites for further reaction with histamine to afford histamine-functionalized CNHs (His-CNHs). Raman spectroscopy, XPS and TGA confirmed successful functionalization. Transmission electron microscopy (TEM) demonstrated that His-CNHs efficiently complex quantum dots (QDs) through imidazole-Zn interactions. Combination of His-CNHs, QDs, and a poly(oligo-(ethylene glycol9) methyl ether methacrylate)-block-poly(4-vinyl imidazole) copolymer using an interfacial complexation technique afforded stable ternary nanocomplexes with average hydrodynamic diameters under 100 nm. These ternary nanocomplexes represent promising materials for photothermal cancer theranostics due to their size and stability. The efficient reaction of 2-isocyanatoethyl methacrylate with amines afforded urea-containing methacrylic monomers, where the amine-derived pendant groups determined the polymer Tg. Reversible addition-fragmentation chain-transfer (RAFT) polymerization enabled the synthesis of ABA triblock copolymers with urea-containing methacrylic outer blocks and poly(2-ethylhexyl methacrylate) inner blocks. These ABA triblocks copolymers displayed composition dependent phase-separated morphologies and desirable mechanical properties. The urea-containing polymers efficiently complexed gold nanoparticles through urea-gold interactions. Furthermore, urea-containing methacrylic polymers served as a useful matrix for incorporation of silica-coated upconverting nanoparticles, affording upconverting nanoparticle composite films.The novel ionene monomer N1,N2-bis(3-(dimethylamino)propyl)oxalamide permitted synthesis of novel oxalamide-containing ammonium ionenes. The hydrogen bonding, charge density, and counter anion tuned the ionene mechanical properties. The ionene structure also influenced water uptake and conductivity. The differences in physical properties correlated well with the morphology observed in small-angle X-ray scattering. The oxalamide-containing ionenes greatly enhance mechanical properties compared to typical ammonium ionenes, and further expand the library of ionene polymers.
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Inglefield, David Lott Jr. "Tailoring Intermolecular Interactions for High-Performance Nanocomposites." Diss., Virginia Tech, 2014. http://hdl.handle.net/10919/64411.

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Acid oxidation of multi-walled carbon nanotubes (MWCNTs) introduced carboxylic acid sites onto the MWCNT surface, which permitted further functionalization. Derivatization of carboxylic acid sites yielded amide-amine and amide-urea functionalized MWCNTs from oxidized precursors. Conventional MWCNT characterization techniques including X-ray photoelectron spectroscopy (XPS), thermogravimetric analysis (TGA), and Raman spectroscopy supported successful MWCNT functionalization. Incorporation of MWCNTs functionalized with hydrogen bonding groups into a segmented polyurethane matrix led to an increase in mechanical properties at optimized MWCNT loadings, in contrast with non-functionalized MWCNTs that resulted in mechanical property decreases across all loadings. Dynamic mechanical analysis (DMA) demonstrated an increase in the polyurethane-MWCNT composite flow temperature with increasing hydrogen bonding MWCNT incorporation, as opposed to non-functionalized MWCNT composites which displayed no significant change in flow temperature. Variable temperature Fourier transform infrared spectroscopy (VT FT-IR) probed temperature-dependent hydrogen bonding in the polyurethane-MWCNT composites and revealed a significant impact on composite hydrogen bonding interactions upon MWCNT incorporation, which was amplified in composites formed using hydrogen bonding functionalized MWCNTs. Acid oxidation of carbon nanohorns (CNHs) yielded carboxylic acid functionalized CNHs, providing sites for further reaction with histamine to afford histamine-functionalized CNHs (His-CNHs). Raman spectroscopy, XPS and TGA confirmed successful functionalization. Transmission electron microscopy (TEM) demonstrated that His-CNHs efficiently complex quantum dots (QDs) through imidazole-Zn interactions. Combination of His-CNHs, QDs, and a poly(oligo-(ethylene glycol9) methyl ether methacrylate)-block-poly(4-vinyl imidazole) copolymer using an interfacial complexation technique afforded stable ternary nanocomplexes with average hydrodynamic diameters under 100 nm. These ternary nanocomplexes represent promising materials for photothermal cancer theranostics due to their size and stability. The efficient reaction of 2-isocyanatoethyl methacrylate with amines afforded urea-containing methacrylic monomers, where the amine-derived pendant groups determined the polymer Tg. Reversible addition-fragmentation chain-transfer (RAFT) polymerization enabled the synthesis of ABA triblock copolymers with urea-containing methacrylic outer blocks and poly(2-ethylhexyl methacrylate) inner blocks. These ABA triblocks copolymers displayed composition dependent phase-separated morphologies and desirable mechanical properties. The urea-containing polymers efficiently complexed gold nanoparticles through urea-gold interactions. Furthermore, urea-containing methacrylic polymers served as a useful matrix for incorporation of silica-coated upconverting nanoparticles, affording upconverting nanoparticle composite films.The novel ionene monomer N1,N2-bis(3-(dimethylamino)propyl)oxalamide permitted synthesis of novel oxalamide-containing ammonium ionenes. The hydrogen bonding, charge density, and counter anion tuned the ionene mechanical properties. The ionene structure also influenced water uptake and conductivity. The differences in physical properties correlated well with the morphology observed in small-angle X-ray scattering. The oxalamide-containing ionenes greatly enhance mechanical properties compared to typical ammonium ionenes, and further expand the library of ionene polymers.
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Robertson, Katherine N. "Intermolecular interactions in a series of organoammonium tetraphenylborates." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 2001. http://www.collectionscanada.ca/obj/s4/f2/dsk3/ftp04/NQ66644.pdf.

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Fortin, Anouk S. "Intra- and intermolecular interactions governing Pax-3 function." Thesis, McGill University, 2001. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=37617.

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Pax-3 is a transcription factors important in normal embryonic development, as highlighted by its mutation in independent alleles of the Splotch mouse mutant and human Waardenburg syndrome, both characterized by pigmentary disturbances in the heterozygous state and limb muscle defects in the homozygotes. Pax-3 contains two structurally independent DNA-binding domains, a paired domain and a homeodomain. Through the analysis of a number of naturally occurring mutations, we have shown that both DNA-binding domains are functionally interdependent, as independent mutations in either domain can affect the DNA-binding activity of the other. In support of this finding, modeling the deleterious mutations into the three dimensional structure of the paired domain suggests that a series of consecutive phosphate contacts are essential for DNA-binding by both the paired domain and homeodomain of Pax-3. In addition, the paired domain can regulate the DNA-binding specificity and dimerization potential of the homeodomain and we have exploited the possibility to transfer this effect to a heterologous homeodomain to identify the protein segments involved in this functional interaction. Characterization of a series of chimeric proteins containing stepwise deletions within the paired domain provided two key findings: (i) the C-terminal subdomain of the paired domain does not play a major role in the regulation of the homeodomain DNA-binding and (ii) the N-terminal subdomain and, in particular, the second alpha-helix are essential for the modulation of homeodomain DNA-binding. In addition to intermolecular interactions, the functional association with other transcription factors can also modulate Pax-3 target gene selection and regulation. We found that Pax-3 can recruit PEA3, a member of the ETS family, to form a ternary complex with DNA sequences containing either a paired domain or homeodomain recognition site and a sub-optimal Ets site to which PEA3 normally does not bind. We have
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Books on the topic "Intermolecular interactions"

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Kaplan, Ilya G. Intermolecular Interactions. Chichester, UK: John Wiley & Sons, Ltd, 2006. http://dx.doi.org/10.1002/047086334x.

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Gans, Werner, and Jan C. A. Boeyens, eds. Intermolecular Interactions. Boston, MA: Springer US, 1998. http://dx.doi.org/10.1007/978-1-4615-4829-4.

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1949-, Gans W., Boeyens J. C. A, and Structural Chemistry Indaba on Molecular Interactions (2nd : 1997 : Kruger National Park, South Africa), eds. Intermolecular interactions. New York: Plenum Press, 1998.

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Gans, Werner. Intermolecular Interactions. Boston, MA: Springer US, 1998.

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Randall, Karen L. Studies of intermolecular interactions. Ottawa: National Library of Canada = Bibliothèque nationale du Canada, 1997.

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Birnbaum, G. Phenomena Induced by Intermolecular Interactions. Boston, MA: Springer US, 1985.

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Birnbaum, G., ed. Phenomena Induced by Intermolecular Interactions. Boston, MA: Springer US, 1985. http://dx.doi.org/10.1007/978-1-4613-2511-6.

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George, Birnbaum, ed. Phenomena induced by intermolecular interactions. New York: Plenum Press, 1985.

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Baev, Alexei K. Specific Intermolecular Interactions of Organic Compounds. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-21622-0.

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service), SpringerLink (Online, ed. Specific Intermolecular Interactions of Organic Compounds. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012.

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Book chapters on the topic "Intermolecular interactions"

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Sommerer, Shaun O. "Intermolecular Interactions." In Intermolecular Interactions, 1–2. Boston, MA: Springer US, 1998. http://dx.doi.org/10.1007/978-1-4615-4829-4_1.

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Boeyens, Jan C. A. "Intermolecular Bonding." In Intermolecular Interactions, 3–7. Boston, MA: Springer US, 1998. http://dx.doi.org/10.1007/978-1-4615-4829-4_2.

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Allen, Frank H. "Relationships Between Experiment and Theory in the Study of Intermolecular Interactions." In Intermolecular Interactions, 111–20. Boston, MA: Springer US, 1998. http://dx.doi.org/10.1007/978-1-4615-4829-4_10.

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Ōsawa, Eiji, Hitoshi Gotō, Takako Sugiki, and Keisuke Imai. "Study of Intermolecular Interactions Using Crystal Structure Database as Reference: A Preliminary Report on the Adjustment of Van Der Waals Constants." In Intermolecular Interactions, 121–34. Boston, MA: Springer US, 1998. http://dx.doi.org/10.1007/978-1-4615-4829-4_11.

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Krüger, Carl, K. Angermund, B. Bartkowska, J. Bruckmann, K. H. Claus, J. Kuhnigk, F. Lutz, and I. Ortmann. "Reactivity in Solid State and Electron Deformation Density Determinations." In Intermolecular Interactions, 135–54. Boston, MA: Springer US, 1998. http://dx.doi.org/10.1007/978-1-4615-4829-4_12.

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Bernal, I., James Cetrullo, Jozef Myrczek, John S. Ricci, D. J. Radanović, and S. R. Trifunović. "Metal Amine Carboxylates as Hydronium Ion Traps. Part 5.1. The Structure of K1/2(H5O2)1/2{(−)D-trans-(O6)-[Co(1,3-SS-pddadp)]}· 2H2O (I) Determined at 18°C and −100°C and of Li{(−)D-trans-(O6)-[Co(1,3-SS-pddadp)]}·7H2O (II) AT 18°C. Intra- and Intermolecular Interactions in the Crystallization of Metal Diamine Carboxylates and on Hydronium Ion Traps." In Intermolecular Interactions, 155–64. Boston, MA: Springer US, 1998. http://dx.doi.org/10.1007/978-1-4615-4829-4_13.

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Amann, Anton. "Chemical Reactions in the Framework of Single Quantum Systems." In Intermolecular Interactions, 9–24. Boston, MA: Springer US, 1998. http://dx.doi.org/10.1007/978-1-4615-4829-4_3.

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Sutcliffe, B. T. "The Molecule and its Environment." In Intermolecular Interactions, 25–48. Boston, MA: Springer US, 1998. http://dx.doi.org/10.1007/978-1-4615-4829-4_4.

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Ogilvie, J. F. "Dynamic Aspects of Intermolecular Interactions." In Intermolecular Interactions, 49–56. Boston, MA: Springer US, 1998. http://dx.doi.org/10.1007/978-1-4615-4829-4_5.

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Koritsánszky, Tibor. "Atomic Interactions and the Charge Density." In Intermolecular Interactions, 57–70. Boston, MA: Springer US, 1998. http://dx.doi.org/10.1007/978-1-4615-4829-4_6.

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Conference papers on the topic "Intermolecular interactions"

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HASKOPOULOS, A., and G. MAROULIS. "INTERMOLECULAR INTERACTIONS OF (H2O)2." In Proceedings of the International Conference (ICCMSE 2003). WORLD SCIENTIFIC, 2003. http://dx.doi.org/10.1142/9789812704658_0050.

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Bermúdez, Celina, and Alberto Li, Lesarri. "INTERMOLECULAR INTERACTIONS OF TOLUNITRILES (CH3C6H4CN)." In 2023 International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2023. http://dx.doi.org/10.15278/isms.2023.7136.

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Astrand, P. O., A. Wallqvist, and G. Karlstrom. "Intermolecular Interactions of Urea and Water." In Advances in biomolecular simulations. AIP, 1991. http://dx.doi.org/10.1063/1.41327.

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Highstrete, Lt Clark, and John Wessel. "Intermolecular Interactions in the Fluorene Dimer." In High Resolution Spectroscopy. Washington, D.C.: Optica Publishing Group, 1993. http://dx.doi.org/10.1364/hrs.1993.pd9.

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Excited state interactions in molecular dimers and higher clusters are of increasing spectroscopic interest because the interactions reveal the nature of the intermolecular potential and provide geometrical information about clusters. Cold clusters were prepared in a supersonic beam and studied by fluorescence excitation and photoionization and spectroscopies. Past studies revealed that benzene dimers are characterized by weak intermolecular interactions in the first excited state, whereas naphthalene dimers undergo strong excimer formation that results in broad electronic spectra. Prior reports2 indicated that fluorene dimers fluoresce efficiently from a lower energy excimer state.
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Stevens, J., P. C. Leung, S. H. Chou, A. J. Freeman, and E. Wimmer. "Intermolecular Interactions And Crystal Stabilities Of Tetrathiafulvalene-Tetracyanoquinodimethane." In 1988 Los Angeles Symposium--O-E/LASE '88, edited by Robert L. Gunshor. SPIE, 1988. http://dx.doi.org/10.1117/12.943967.

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Byrne, Hugh J. "Intermolecular interactions in molecular systems: pros and cons." In OPTO Ireland, edited by Thomas J. Glynn. SPIE, 2003. http://dx.doi.org/10.1117/12.463958.

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Meindinyo, Remi-Erempagamo T., and Thor Martin Svartås. "Intermolecular Forces in Clathrate Hydrate Related Processes." In ASME 2015 34th International Conference on Ocean, Offshore and Arctic Engineering. American Society of Mechanical Engineers, 2015. http://dx.doi.org/10.1115/omae2015-41774.

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The thermodynamics and kinetics of clathrate hydrate formation processes are topics of high scientific interest, especially in the petroleum industry. Researchers have made efforts at understanding the underlying processes that explicate the macroscopic observations from experiments and other research methods of gas hydrate formation. To achieve this, they have employed theories founded upon force related intermolecular interactions. Some of the theories and concepts employed include hydrogen bonding, the Leonard Jones force principle, and steric interactions. This paper gives a brief review of how these intermolecular interaction principles have been understood, and used as tools, in explaining the inaccessible microscopic processes, that characterize clathrate hydrate formation. It touches upon nucleation, growth, and inhibition processes.
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Sanz, M., Jackson Tang, Elena Alonso, Isabel Peï¾–a, Donatella Loru, Ecaterina Burevschi, Shefali Saxena, and S. Murugachandran. "INTERMOLECULAR NON-COVALENT INTERACTIONS REVEALED BY BROADBAND ROTATIONAL SPECTROSCOPY." In 74th International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2019. http://dx.doi.org/10.15278/isms.2019.tb01.

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Voycheva, Christina. "INTERMOLECULAR INTERACTIONS IN BIOPOLYMER COMPOSITES STUDIED BY IR SPECTROSCOPY." In 13th SGEM GeoConference NANO, BIO AND GREEN � TECHNOLOGIES FOR A SUSTAINABLE FUTURE. Stef92 Technology, 2013. http://dx.doi.org/10.5593/sgem2013/bf6/s25.014.

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Blaszczak, Zdzislaw, Marek Halas, Iwona Iwaszkiewicz-Kostka, and Wiktor Prezdo. "Intermolecular interactions in n,n-dimethylnitramine solutions in benzene." In Laser Technology VI, edited by Wieslaw L. Wolinski and Zdzislaw Jankiewicz. SPIE, 2000. http://dx.doi.org/10.1117/12.405994.

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Reports on the topic "Intermolecular interactions"

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Novoa, J. J., Myung-Hwan Whangbo, and J. M. Williams. Intermolecular interactions involving C-H bonds, 3, Structure and energetics of the interaction between CH{sub 4} and CN{sup {minus}}. Office of Scientific and Technical Information (OSTI), December 1991. http://dx.doi.org/10.2172/10187953.

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George, Thomas F., Lahsen Assoufid, G. A. Mansoori, and Guoping Zhang. Diamond-Like and Self-Assembling Organic Nanostructures: Measurement and Simulation of Intermolecular Interactions and Structural Characteristics. Fort Belvoir, VA: Defense Technical Information Center, September 2008. http://dx.doi.org/10.21236/ada498551.

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Jayaraman, Arthi. Final Report: Predictive coarse-grained (CG) modeling of morphologies in polymer nanocomposites with specific and directional intermolecular interactions. Office of Scientific and Technical Information (OSTI), May 2022. http://dx.doi.org/10.2172/1868045.

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