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Relevant bibliographies by topics / Water dimer

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Academic literature on the topic 'Water dimer'

Author: Grafiati

Published: 4 June 2021

Last updated: 5 February 2022

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Journal articles on the topic "Water dimer"

1

Malomuzh, M. P., and V. M. Makhlaichuk. "Dimerization Degree of Water Molecules, Their Effective Polarizability, and Heat Capacity of Saturated Water Vapor." Ukrainian Journal of Physics 63, no. 2 (March 10, 2018): 121. http://dx.doi.org/10.15407/ujpe63.2.121.

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The properties of water vapor have been studied. The main attention is focused on the physical nature of the effective polarizability of water vapor and the heat capacity of water vapor at a constant volume, with a proper modeling of those parameters being a good test for a correct description of the dimer concentration in various approaches. Thermal vibrations of water dimers are found to be the main factor governing the specific temperature dependences of those characteristics, and the normal coordinates of dimer vibrations are determined. Fluctuations of the dipole moments of dimers and their contribution to the dielectric permittivity of water vapor are considered in detail. The contribution of the interparticle interaction to the heat capacity is taken into account. By analyzing the effective polarizability and the heat capacity, the temperature dependence of the dimer concentration at the vapor-liquid coexistence curve is determined. The noticeable dimerization in saturated water vapor takes place only at temperatures T/Tc > 0.8, where Tc is the critical temperature.

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Bertran, J., M. F. Ruiz-L�pez, D. Rinaldi, and J. L. Rivail. "Water dimer in liquid water." Theoretica Chimica Acta 84, no. 3 (November 1992): 181–94. http://dx.doi.org/10.1007/bf01113207.

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Li, Xiao Yi, and Leif A. Eriksson. "Molecular dynamics study of lignin constituents in water." Holzforschung 59, no. 3 (May 1, 2005): 253–62. http://dx.doi.org/10.1515/hf.2005.042.

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Abstract Molecular dynamics simulations were used to explore the distribution of linkages in coumaryl alcohol and coniferyl alcohol systems, including monomeric systems and monomers interacting with β-O4 dimers, respectively. Studying the interactions of two monolignols and the corresponding dimers sheds light on the preferred mechanism of reaction of the growing lignin polymer from the view of kinetic factors. The energy change upon association was quantified, and the distances between the centers of mass of different molecules, and the relative orientations between the phenol groups were calculated for all the systems. Using a cut-off threshold of 4 Å to indicate association leading to bond formation, it is concluded that the presence of the additional methoxy group on coniferyl alcohol assists in promoting interaction of the O4 group with the second moiety. Based on the computed data it is furthermore concluded that in aqueous solution, the most likely model of polymerization is that involving initial dimer formation, followed by dimer-dimer association.

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Apelblat, Alexander. "Dimerization and continuous association including formation of cyclic dimers." Canadian Journal of Chemistry 69, no. 4 (April 1, 1991): 638–47. http://dx.doi.org/10.1139/v91-097.

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New aspects of the theory of ideal associated mixtures related to a differentiation between formed cyclic and linear dimers are discussed. A mathematical analysis is presented for the dimerization model, A + B + A2, the continuous association (Mecke–Kempter) model, [Formula: see text], both coupled with the cyclic dimmer → linear dimer transformation and for the unsymmetrical (mixed) dimer formation model, A + B + A2 + B2 + AB. Introduction of the standard reaction enthalpies and volumes associated with transformations of dimers leads to a considerable change in behavior and symmetry properties of the excess thermodynamic functions. In terms of the modified Mecke–Kempter model, a consistent representation of the excess Gibbs energy of mixing GE, heat of mixing HE, and excess molar volume VE is reported for the acetic acid – water system at 298.15 K. Key words: association, dimerization, linear dimers, cyclic dimers, hydrogen bonding, carboxylic acids, alcohols, aqueous solutions.

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Malomuzh, N. P., V. N. Makhlaichuk, and S. V. Khrapatyi. "Water dimer dipole moment." Russian Journal of Physical Chemistry A 88, no. 8 (July 18, 2014): 1431–35. http://dx.doi.org/10.1134/s0036024414080172.

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Wijaya, Karna, Oliver Moers, Armand Blaschette, and Peter G. Jones. "Polysulfonylamine, XC [1] Carbonsäure-Dimere, Wasser-Dimere und 18-Krone-6-Moleküle als Baugruppen eines supramolekularen Kettenpolymers: Darstellung und Struktur von (CH2CH2O)6 • 4H2O • 2HN(SO2C6H4-4-COOH)2 / Polysulfonylamines, XC [1] Carboxylic Acid Dimers, Water Dimers and 18-Crown-6 Molecules as Building Blocks in a Supramolecular Chain Polymer: Synthesis and Structure of (CH2CH2O)6 · 4H2O · 2HN(SO2C6H4-4-COOH)2." Zeitschrift für Naturforschung B 52, no. 8 (August 1, 1997): 997–1002. http://dx.doi.org/10.1515/znb-1997-0821.

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The ternary title complex (2) is readily obtained by co-crystallization of 18-crown-6 (18C6) and di(4-carboxybenzenesulfonyl)amine (1) from hot water and was characterized by low-temperature X-ray diffraction. The crystal structure (triclinic, space group P1̄) displays one-dimensional polymeric sequences [(H2O)2···18C6···(H2O)2···{HN(SO2C6H4-4-COOH)2}2] in which the molecules are associated through seven independent hydrogen bonds. The 18C6 ring lies on a crystallographic inversion centre and adopts the common pseudo-D3d conformation. On both sides, the ring is flanked by a strongly hydrogen-bonded water dimer H2O-H-OH. This species forms three weak O-H-O bonds to alternating ether oxygen atoms and accepts a strong N-H-O bond from the adjacent acid dimer (1)2. The water dimers thus act as ideal donor-acceptor balancing links between the hexafunctional polyether and the monofunctional NH groups of the (1)2 dimers. The (1)2 dimer itself is formed by two symmetry related cyclic O-H···O interactions (both H disordered) of the well-known carboxylic acid dimer type. To this effect, molecule 1 adopts a folded, pseudo-Cs symmetric conformation with stacked carboxyphenyl groups.

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Ruscic, Branko. "Active Thermochemical Tables: Water and Water Dimer." Journal of Physical Chemistry A 117, no. 46 (July 8, 2013): 11940–53. http://dx.doi.org/10.1021/jp403197t.

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Goebbert, Daniel J., and Paul G. Wenthold. "Water Dimer Proton Affinity from the Kinetic Method: Dissociation Energy of the Water Dimer." European Journal of Mass Spectrometry 10, no. 6 (December 2004): 837–45. http://dx.doi.org/10.1255/ejms.684.

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Bartlett, Stuart A., Emma V. Sackville, Emma K. Gibson, Veronica Celorrio, Peter P. Wells, Maarten Nachtegaal, Stafford W. Sheehan, and Ulrich Hintermair. "Evidence for tetranuclear bis-μ-oxo cubane species in molecular iridium-based water oxidation catalysts from XAS analysis." Chemical Communications 55, no. 54 (2019): 7832–35. http://dx.doi.org/10.1039/c9cc02088h.

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Quek, Puay Hoon, and Jiangyong Hu. "Effects of wavelengths of medium-pressure ultraviolet radiation on photolyase and subsequent photoreactivation." Water Supply 13, no. 1 (February 1, 2013): 158–65. http://dx.doi.org/10.2166/ws.2012.087.

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This study aims to investigate the effect of different wavelengths (254, 266, 280 and 365 nm) in polychromatic medium-pressure (MP) UV radiation on the ability of photolyases in repairing dimers and discusses its impact on subsequent photoreactivation. Photolyase was exposed to various doses and irradiances of the UV wavelengths and the dimer repair abilities of the irradiated photolyase were determined via a spectrophotometric assay. At wavelengths below 300 nm, dimer repair rates were not influenced by the UV irradiation between 0.03 and 0.10 mW cm−2. For 365 nm, photolyase exhibited enhanced dimer repair at 0.05 mW cm−2 and then reduced dimer repair with increasing irradiance. In addition, photolyase was found to have decreasing dimer repair rates when exposed to increasing UV doses at all tested wavelengths. Lower photoreactivation levels after MP UV disinfection as compared to low-pressure (LP) UV disinfection was not attributable to a single wavelength in the polychromatic radiation, but is possibly due to the simultaneous exposure of photolyase to a broad spectrum of radiation, which led to a reduction in the dimer repair ability of photolyase. This study is the first to report the direct effects of UV radiation on photolyase enzyme. The data in the study provide some evidence for the mechanism for which MP UV disinfection suppresses photoreactivation in Escherichia coli, which has only been speculated on so far. The knowledge from this study will provide a basis upon which to investigate other enzymes involved in the repair of UV damage to DNA.

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Dissertations / Theses on the topic "Water dimer"

1

L'Écuyer, Tristan Simon. "Water dimer atmospheric absorption." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1997. http://www.collectionscanada.ca/obj/s4/f2/dsk3/ftp05/mq24864.pdf.

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Bieker, Helen [Verfasser]. "Dissociation dynamics of size-selected water dimer / Helen Bieker." Hamburg : Staats- und Universitätsbibliothek Hamburg Carl von Ossietzky, 2020. http://d-nb.info/1230561943/34.

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Toledo, Evelyn Jeniffer de Lima. "Aplicação do campo elétrico em dímeros de água." Universidade de São Paulo, 2011. http://www.teses.usp.br/teses/disponiveis/75/75131/tde-25102011-171500/.

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A água, conhecida como solvente universal, participa da maioria das reações químicas e composições biológicas, tem importância vital em nosso planeta, tornando a vida como conhecemos inconcebível sem a sua presença. Tais propriedades advêm da forma como as moléculas interagem entre si, e a principal ligação química existente é a ligação de hidrogênio. Portanto, compreender como ela acontece e ser capaz de manipulá-la pode ser considerada uma importante técnica na busca de novos comportamentos. Esta dissertação visa compreender como o campo elétrico nas suas variantes: direção, sentido e intensidade podem afetar a água. Sendo tal estudo realizado através de cálculos utilizando métodos de química quântica: Teoria do Funcional da Densidade e a Teoria de Perturbação Moller-Plesset de segunda ordem. Como resultado obteve-se que quando o campo elétrico é aplicado em uma direção e sentido fora do plano da ligação de hidrogênio, a estrutura inicial tende a se rearranjar produzindo uma estrutura mais fracamente ligada do que a ordinária. Quando aplicamos o campo no plano da ligação de hidrogênio, temos resultados mais pronunciados, sendo que, se o sentido for : Doador -> Receptor a estrutura resultante estará mais fracamente ligada e se o sentido for Receptor -> Doador a estrutura produzida estará mais fortemente ligada. Os resultados obtidos mostram também que tais mudanças acontecem principalmente devido a alterações eletrostáticas, como mudança na densidade de carga da ligação de hidrogênio. Também confirmou-se um ponto crítico no campo 0,15 V/Å, como sugerido na literatura. Esta singularidade foi atribuída neste trabalho à uma transição estrutural. O campo também modificou a importância das interações secundárias, principalmente entre os átomos de oxigênio, e ao desligá-lo, o sistema tende a voltar ao estado inicial.
The water is know as the universal solvent, part of most chemical reactions and biological compositions, it is vitally important to our planet, making life as we know it inconceivable without its presence. These properties arise from how the molecules interact, and the main existing chemical link is the hydrogen bond. Therefore, to understand how this happens and be able to manipulate it can be considered an important technique in the search for new behaviors. Thus, this paper aims to understand how the electric field in its variants: direction, sense and intensity can affect the water. This study is undertaken through calculations using quantum chemistry methods: Density Functional Theory and Moller-Plesset Perturbation Theory to Second Order. As a result was found that when the electric field is applied in direction and sense out of the plane of the hydrogen bond, the initial structure tends to rearrange itself to produce a more loosely bound than the ordinary. When the electric field is applied in the hydrogen bond plane, the have results obtained are more pronounced. Sense is: Donor -> Receiver initial structure will be more loosely connected and that when the sense is Receiver -> Donor initial structure will be tightly linked. Our results also show that such changes occur mainly due to electrostatic changes, mainly in the change in the charge density of hydrogen bond. It was also confirmed a critical point in the field 0, 15 V / Å, as suggested by Vegiri. This was attributed to a structural transition. The field also changed the importance of secondary interactions, especially between the oxygen atoms. And when the field is shutdown the system tends back to its to initial structure.

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Benedek, Nicole Ann, and n. benedek@gmail com. "Interactions in ionic molecular crystals." RMIT University. Applied Sciences, 2006. http://adt.lib.rmit.edu.au/adt/public/adt-VIT20070109.161440.

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We have used ab initio computational simulation techniques to investigate both intra- and intermolecular interactions in a novel family of ionic organophosphonate molecular crystals. We have examined the influence of various numerical approximations on the computed geometry and binding energies of a selection of well-characterised hydrogen bonded systems. It was found that numerical basis sets provided the efficiency required to study the large hydrogen bonded dimer anions present in the organophosphonate system, while also producing accurate geometries and binding energies. We then calculated the relaxed structures and binding energies of phenylphosphonic acid dimer in the two arrangements in which it is present in the bulk crystal. The computed geometries were in excellent agreement with the experimental structures and the binding energies were consistent with those found for other ionic hydrogen bonded systems. Electron density maps were used to gain insight into the nature of the hydrogen bonding interaction between phenylphosphonic acid dimers. We also examined the effect of aromatic ring substituents on the geometry and energetics of the hydrogen bonding interaction. The nitro-substituted dimer was predicted to have a stronger binding energy than its unsubstituted parent while the methyl-substituted dimer was predicted to have a similar binding energy to its unsubstituted parent. An analysis of crystal field effects showed that the structure of the phenylphosphonic acid dimers in the organophosphonates is a complex product of competing intra- and intermolecular forces and crystal field effects. Cooperative effects in the organophosphonate system were also investigated and it was found that the interactions were mostly one-body (local) in nature. We have examined the intramolecular charge-transfer interaction between copper-halogen cations in the organophosphonate materials. The origin of geometric differences between the Cu(I) starting material and Cu(II) product cations was attributed to the electronic configuration of the Cu ion, not crystal field effects. To gain further insight into the difference in electronic structure between the starting material and product, we attempted to simulate the step-by-step dissociation of the [CuI]+ system. Although this investigation was not successful, we were able to expose some of the pitfalls of simulating dissociating odd-electron systems. We also analysed and compared the charge-transfer interaction in the chloro-, bromo- and iodo-forms of the organophosphonate family. The charge-transfer interaction was predicted to increase on going from the chloro- to the iodo-form, consistent with solid-state UV-visible data. Finally, we used the highly accurate Quantum Monte Carlo (QMC) method to investigate the hydrogen bonding interaction in water dimer and to calculate the dissociation energy. The accuracy of the experimental estimate for the dissociation energy has recently been questioned and an alternative value has been put forward. Our results lend support to the validity of the alternative value and are also in excellent agreement with those from other high-level calculations. Our results also indicate that QMC techniques are a promising alternative to traditional wavefunction techniques in situations where both high accuracy and efficiency are important.

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Cho, Hyung Min. "A full-dimensional quantum Monte Carlo study of H5O2+." Connect to this title online, 2004. http://rave.ohiolink.edu/etdc/view?acc%5Fnum=osu1085048780.

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Thesis (Ph. D.)--Ohio State University, 2004.
Title from first page of PDF file. Document formatted into pages; contains xii, 88 p.; also includes graphics (some col.). Includes bibliographical references (p. 83-88). Available online via OhioLINK's ETD Center

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Sichula, Vincent A. "Flavins and Their Analogues as Natural and Artificial Catalysts." Bowling Green State University / OhioLINK, 2011. http://rave.ohiolink.edu/etdc/view?acc_num=bgsu1294288149.

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7

Poirel, Arnaud. "Synthèse et étude d'une nouvelle génération de colorants borondipyrrométhènes (BODIPYs) émettant dans le rouge et le proche infrarouge pour des applications biologiques." Phd thesis, Université de Strasbourg, 2014. http://tel.archives-ouvertes.fr/tel-01037995.

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Au cours de ces travaux de thèse, la synthèse de BODIPYs émettant dans le rouge et le proche infrarouge a été réalisée. Un premier travail d'extension de la conjugaison électronique (soit par introduction de groupements aromatiques sur le corps du BODIPY, soit par dimérisation) a permis d'atteindre les basses énergies du spectre électromagnétique. La validation d'une méthode de synthèse de BODIPYs à l'aide d'orthoesters a permis une mise en oeuvre aisée et une nette amélioration de leurs rendements. Parmi les fluorophores obtenus, les dithiényl-BODIPYs émettant dans la fenêtre thérapeutique (650-900 nm) présentent des propriétés optiques et électrochimiques intéressantes. Ils ont été utilisés pour des applications dans le domaine biologique. Après leur solubilisation dans les milieux aqueux par introduction de groupements ammoniums, la détection d'un acide aminé, la cystéine, a pu être réalisée par spectroscopies d'absorption et de fluorescence mettant en évidence un système ratiométrique. De plus, le marquage d'une protéine modèle, le sérum d'albumine bovine, permet d'envisager l'utilisation de ce type de BODIPYs pour l'imagerie biologique grâce à un rendement quantique de fluorescence élevé en milieu physiologique.

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Boyle, Susan Patricia. "A study of air-to-water sound transmission, with application to semi-closed circuit diver breathing apparatus." Thesis, University of Southampton, 1994. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.241040.

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Schlesinger, Martin [Verfasser], Walter [Akademischer Betreuer] Strunz, and Volker [Akademischer Betreuer] Engel. "Quantum Dissipative Dynamics and Decoherence of Dimers on Helium Droplets / Martin Schlesinger. Gutachter: Walter Strunz ; Volker Engel. Betreuer: Walter Strunz." Dresden : Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2012. http://d-nb.info/1067729917/34.

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Marshall, Tracey. "Dynamic chemistry : nucleobase recognition by synthetic receptors and cis-trans acylhydrazone isomerism." Thesis, Bordeaux 1, 2012. http://www.theses.fr/2012BOR14477/document.

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Chimie dynamique: reconnaissance de nucléobases par des récepteurs synthétiques et isomérie cis-trans d'hydrazones acylées.Ce travail traite du développement des systèmes moléculaires qui peuvent s'adapter à l'addition de substances qui agissent comme un gabarit. Cette approche permet d'isoler une espèce majeure à partir d'un mélange de composés par le biais de la chimie combinatoire dynamique (CCD). La première partie de ma thèse de doctorat inclus l'utilisation d'un ADN simple brin (ADNsb) comme un gabarit pour le transfert d'information par auto-assemblage de récepteurs sans avoir besoin d'enzyme. De nouveaux récepteurs de l'adénine et de la guanine (pinces A et G) solubles dans l'eau ont été conçues dans ce but. Une approche utilisant la résonance magnétique nucléaire (RMN) a été utilisée pour déterminer l'affinité de liaison comme preuve d'une reconnaissance spécifique et efficace. Une évaluation dans l'eau par dichroïsme circulaire (CD) et mesure de la température de fusion par UV (Tm) a été réalisée. Cela a permis de tester respectivement la capacité d'auto-assemblage entre les pinces et un modèle ADNsb, et la force du processus de coopérativité. La deuxième partie de ce travail est axée sur le tri spontanné de motifs pyridine acylhydrazone et sur les configurations intéressantes qu'ils adoptent. Nous avons étudié la synthèse d'une série de motifs pyridine acylhydrazone: dimère, trimères et pentamères. Des études RMN ont permis d'évaluer les changements dans l'équilibre configurationnel cis / trans de ces systèmes dynamiques. Les études ont montré que l'équilibre attendu est biaise la cis acylhydrazone pyridine isomère a été observée par diffraction des rayons X
Dynamic chemistry: nucleobase recognition by synthetic receptors and cis-trans acylhydrazone isomerism. This work deals with the development of molecular systems which can adapt upon the addition of substances that act as templates. This approach enables one major species to be identified from a mixture of compounds through the use of dynamic combinatorial chemistry (DCC). The first part of my PhD included the use of a single stranded DNA (ssDNA) as a template for information transfer via the self-assembly of receptors without the need for enzymes. New water soluble adenine and guanine receptors (A and G clamps) were designed and synthesised for this purpose. Nuclear magnetic resonance (NMR) titration studies were carried out to calculate the binding affinity and as a proof of specific and efficient recognition. An assessment in water via circular dichroism (CD) and UV temperature melting (Tm) studies was carried out. This tested the ability for self-assembly between the clamps and a ssDNA template and the strength of the cooperative process respectively. The second part of my PhD focused on the self-sorting of acylhydrazone pyridine motifs and the interesting configurations they adopt. The feasibility to synthesise these acylhydrazone pyridine motifs (dimer, trimers and pentamers) was investigated. X-ray and NMR studies showed that the equilibrium was found to be biased in an unusual way, and the cis acylhydrazone pyridine isomer was observed

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Books on the topic "Water dimer"

1

International, Scuba Schools. Open water diver. [S.l.]: Concept Systems Inc., 1990.

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Betts, Edward A. Open water sport diver. [Freeport, N.Y.]: ANDI International, 1999.

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Instructors, Professional Association of Diving. Open water diver manual. Rancho Santa Margarita, CA: PADI, 1999.

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Professional Association of Diving Instructors. Go dive: Open water diver course : multilingual lesson guides. 2nd ed. Rancho Santa Margarita, CA: PADI, 2001.

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Dime cómo flotan los barcos? New York: F. Watts, 1999.

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Gerteis, Klaus. Buffalo Bill und die "verfolgte Unschuld" Groschenhefte von 1871 bis ca. 1930 aus den Mappen von Dr. Walter Gerteis: Eine Ausstellung in der Universitätsbibliothek Trier. Trier: Bibliothekszentrale der Universität Trier, 1999.

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Clinchy. Open Water Diver. 2nd ed. Jones & Bartlett Pub, 2005.

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International, Scuba Schools, ed. Open water diver manual. Fort Collins, CO: Scuba Shools International, 2002.

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Richardson, Drew. Open Water Diver Manual. 2nd ed. PADI, 2005.

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Open Water Diver Manual. Concept Systems, Inc., 2002.

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Book chapters on the topic "Water dimer"

1

Vogt, J. "815 H4O2 Water dimer." In Asymmetric Top Molecules. Part 3, 443–49. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-14145-4_237.

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Wales, David J. "Rearrangements of Water Dimer and Hexamer." In Theory of Atomic and Molecular Clusters, 86–110. Berlin, Heidelberg: Springer Berlin Heidelberg, 1999. http://dx.doi.org/10.1007/978-3-642-58389-6_4.

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Panhuis, M. In Het, R. W. Munn, P. L. A. Popelier, and W. J. Blau. "Distributed Response Analysis of the Water Dimer." In Nonlinear Optics for the Information Society, 107–10. Dordrecht: Springer Netherlands, 2001. http://dx.doi.org/10.1007/978-94-015-1267-1_21.

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Kumagai, Takashi. "Water Dimer: Direct Observation of Hydrogen-Bond Exchange." In Visualization of Hydrogen-Bond Dynamics, 53–65. Tokyo: Springer Japan, 2012. http://dx.doi.org/10.1007/978-4-431-54156-1_5.

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Abdoul-Carime, H., A. Wakisaka, Y. Bouteiller, C. Desfrancois, and J. P. Schermann. "Rigid or floppy water-containing dipole-bound dimer anions." In Small Particles and Inorganic Clusters, 55–61. Berlin, Heidelberg: Springer Berlin Heidelberg, 1997. http://dx.doi.org/10.1007/978-3-642-60854-4_14.

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Kim, Kwang S., and Jongseob Kim. "Structure, Spectra, and Thermodynamic Energies of the Water Dimer and Hexamer." In Recent Theoretical and Experimental Advances in Hydrogen Bonded Clusters, 109–17. Dordrecht: Springer Netherlands, 2000. http://dx.doi.org/10.1007/978-94-015-9434-9_9.

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Avoird, Ad, and Paul E. S. Wormer. "Tunneling Motions and Spectra of Hydrogen Bonded Complexes; The Ammonia Dimer and the Water Trimer." In Recent Theoretical and Experimental Advances in Hydrogen Bonded Clusters, 129–53. Dordrecht: Springer Netherlands, 2000. http://dx.doi.org/10.1007/978-94-015-9434-9_11.

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Brill, Michael, Oriol Vendrell, and Hans-Dieter Meyer. "Shared Memory Parallelization of the Multiconfiguration Time-Dependent Hartree Method and Application to the Dynamics and Spectroscopy of the Protonated Water Dimer." In Advances in the Theory of Atomic and Molecular Systems, 67–80. Dordrecht: Springer Netherlands, 2009. http://dx.doi.org/10.1007/978-90-481-2985-0_4.

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Slanina, Z. "Towards Fully Non-Empirical Understanding of Water-Vapour Non-Ideality: Quantum-Chemical Evaluation of Equilibrium Thermodynamics and Kinetics of the Water Dimer and of the Second Virial Coefficient of Steam." In Proceedings of the 10th International Conference on the Properties of Steam, 350–59. Boston, MA: Springer US, 1986. http://dx.doi.org/10.1007/978-1-4684-7676-7_33.

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Faubel, Manfred. "Liquid Micro Jet Studies of the Vacuum Surface of Water and of Chemical Solutions by Molecular Beams and by Soft X-Ray Photoelectron Spectroscopy." In Molecular Beams in Physics and Chemistry, 597–630. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-63963-1_26.

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AbstractLiquid water, with a vapor pressure of 6.1 mbar at freezing point, is rapidly evaporating in high vacuum, rapidly cooling off by the evaporative cooling, and is freezing to ice almost instantly. Nevertheless, liquid water free vacuum surfaces can be prepared for short instances when injecting very small, fast flowing, liquid jets into high vacuum. They provide perfectly suited targets for molecular beams analysis of molecular evaporation of monomers and dimers from liquids. Also, the microjet technology allows ultrahigh vacuum studies of atomic scale liquid surface composition and electronic structures, as will be demonstrated by using highly focused Synchrotron radiation for EUV/XUV-photoelectron spectrocopy on a wide range of chemical solutions.

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Conference papers on the topic "Water dimer"

1

Mead, Griffin, Geoffrey Blake, Brandon Carroll, and Ian Finneran. "MICROWAVE SPECTRUM OF THE ISOPROPANOL-WATER DIMER." In 71st International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2016. http://dx.doi.org/10.15278/isms.2016.wc09.

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Carroll, Brandon, Geoffrey Blake, and Ian Finneran. "MICROWAVE SPECTROSCOPY OF THE CYCLOPENTANOL - WATER DIMER." In 70th International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2015. http://dx.doi.org/10.15278/isms.2015.rh08.

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3

Sarka, János, Edit Mátyus, and Attila Császár. "ROVIBRATIONAL QUANTUM DYNAMICS OF THE METHANE-WATER DIMER." In 72nd International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2017. http://dx.doi.org/10.15278/isms.2017.td05.

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4

Finneran, Ian, Geoffrey Blake, Marco Allodi, and Brandon Carroll. "HYDROGEN-BONDING AND HYDROPHOBIC INTERACTIONS IN THE ETHANOL-WATER DIMER." In 70th International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2015. http://dx.doi.org/10.15278/isms.2015.rh09.

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5

Kuo, Jer-Lai, and Ying-Cheng Li. "BINDING BETWEEN NOBEL GAS ATOMS AND PROTONATED WATER MONOMER AND DIMER." In 70th International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2015. http://dx.doi.org/10.15278/isms.2015.fc02.

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Karthik, C., Adbhut Gupta, Aditya Joshi, V. Manjuladevi, Raj Kumar Gupta, Mahesh C. Varia, and Sandeep Kumar. "Formation of H-type liquid crystal dimer at air-water interface." In SOLID STATE PHYSICS: Proceedings of the 58th DAE Solid State Physics Symposium 2013. AIP Publishing LLC, 2014. http://dx.doi.org/10.1063/1.4872844.

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7

Slanina, Z. "A Comparison of BJH- and MCYL-Type Potentials on the Water Dimer." In Advances in biomolecular simulations. AIP, 1991. http://dx.doi.org/10.1063/1.41341.

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Carrington, Tucker, and Xiao-Gang Wang. "A NUMERICALLY EXACT FULL-DIMENSIONAL CALCULATION OF RO-VIBRATIONAL LEVELS OF WATER DIMER." In 72nd International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2017. http://dx.doi.org/10.15278/isms.2017.mi07.

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Janik, Ireneusz, and G. Tripathi. "TRANSIENT RAMAN SPECTRA, STRUCTURE AND THERMOCHEMISTRY OF THE SELENOCYANATE DIMER RADICAL ANION IN WATER." In 73rd International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2018. http://dx.doi.org/10.15278/isms.2018.fa05.

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Janik, Ireneusz, Ian Carmichael, and G. Tripathi. "TRANSIENT RAMAN SPECTRA, STRUCTURE AND THERMOCHEMISTRY OF THE THIOCYANATE DIMER RADICAL ANION IN WATER." In 72nd International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2017. http://dx.doi.org/10.15278/isms.2017.fc04.

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Reports on the topic "Water dimer"

1

Wung, A. Simulated X-Ray Absorption Spectroscopy on the Water Dimer. Office of Scientific and Technical Information (OSTI), February 2004. http://dx.doi.org/10.2172/826722.

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Pelton, Jerry D. Through-Water Diver Communication System Test and Evaluation. Fort Belvoir, VA: Defense Technical Information Center, March 1988. http://dx.doi.org/10.21236/ada199797.

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Leyva, Fernando F., and George S. Goehring. Evaluation of a Diver Cooling System for Use With Personal Protective Equipment in Contaminated Water Diving. Fort Belvoir, VA: Defense Technical Information Center, January 2004. http://dx.doi.org/10.21236/ada442725.

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