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Готові списки джерел за темами / Hydrogen bonding

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Добірка наукової літератури з теми "Hydrogen bonding"

Автор: Grafiati

Опубліковано: 4 червня 2021

Оновлено: 25 липня 2025

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Статті в журналах з теми "Hydrogen bonding"

1

Breugst, Martin, Daniel von der Heiden та Julie Schmauck. "Novel Noncovalent Interactions in Catalysis: A Focus on Halogen, Chalcogen, and Anion-π Bonding". Synthesis 49, № 15 (2017): 3224–36. http://dx.doi.org/10.1055/s-0036-1588838.

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Noncovalent interactions play an important role in many biological and chemical processes. Among these, hydrogen bonding is very well studied and is already routinely used in organocatalysis. This Short Review focuses on three other types of promising noncovalent interactions. Halogen bonding, chalcogen bonding, and anion-π bonding have been introduced into organocatalysis in the last few years and could become important alternate modes of activation to hydrogen bonding in the future.1 Introduction2 Halogen Bonding3 Chalcogen Bonding4 Anion-π Bonding5 Conclusions

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2

Wang, Xinyu, Huiyuan Wang, Hongmin Zhang, Tianxi Yang, Bin Zhao, and Juan Yan. "Investigation of the Impact of Hydrogen Bonding Degree in Long Single-Stranded DNA (ssDNA) Generated with Dual Rolling Circle Amplification (RCA) on the Preparation and Performance of DNA Hydrogels." Biosensors 13, no. 7 (2023): 755. http://dx.doi.org/10.3390/bios13070755.

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DNA hydrogels have gained significant attention in recent years as one of the most promising functional polymer materials. To broaden their applications, it is critical to develop efficient methods for the preparation of bulk-scale DNA hydrogels with adjustable mechanical properties. Herein, we introduce a straightforward and efficient molecular design approach to producing physically pure DNA hydrogel and controlling its mechanical properties by adjusting the degree of hydrogen bonding in ultralong single-stranded DNA (ssDNA) precursors, which were generated using a dual rolling circle amplif

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3

Li, Zhangkang, Cheng Yu, Hitendra Kumar, et al. "The Effect of Crosslinking Degree of Hydrogels on Hydrogel Adhesion." Gels 8, no. 10 (2022): 682. http://dx.doi.org/10.3390/gels8100682.

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The development of adhesive hydrogel materials has brought numerous advances to biomedical engineering. Hydrogel adhesion has drawn much attention in research and applications. In this paper, the study of hydrogel adhesion is no longer limited to the surface of hydrogels. Here, the effect of the internal crosslinking degree of hydrogels prepared by different methods on hydrogel adhesion was explored to find the generality. The results show that with the increase in crosslinking degree, the hydrogel adhesion decreased significantly due to the limitation of segment mobility. Moreover, two simple

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4

Ghafouri, Reza, Fatemeh Ektefa, and Mansour Zahedi. "Characterization of Hydrogen Bonds in the End-Functionalized Single-Wall Carbon Nanotubes: A DFT Study." Nano 10, no. 03 (2015): 1550036. http://dx.doi.org/10.1142/s1793292015500368.

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A systematic computational study is carried out to shed some light on the structure of semiconducting armchair single-wall carbon nanotubes (n, n) SWCNTs, n = 4, 5 and 6, functionalized at the end with carboxyl (– COOH ) and amide (– CONH 2) from the viewpoint of characterizing the intramolecular hydrogen bondings at the B3LYP/6-31++G(d, p) level. Geometry parameters display different types of intramolecular hydrogen bonding possibilities in the considered functionalized SWCNTs. All of the hydrogen bondings are confirmed by natural bonding orbitals (NBO) analysis as well as nuclear magnetic re

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5

Dai, Bailin, Ting Cui, Yue Xu, et al. "Smart Antifreeze Hydrogels with Abundant Hydrogen Bonding for Conductive Flexible Sensors." Gels 8, no. 6 (2022): 374. http://dx.doi.org/10.3390/gels8060374.

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Recently, flexible sensors based on conductive hydrogels have been widely used in human health monitoring, human movement detection and soft robotics due to their excellent flexibility, high water content, good biocompatibility. However, traditional conductive hydrogels tend to freeze and lose their flexibility at low temperature, which greatly limits their application in a low temperature environment. Herein, according to the mechanism that multi−hydrogen bonds can inhibit ice crystal formation by forming hydrogen bonds with water molecules, we used butanediol (BD) and N−hydroxyethyl acrylami

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6

Kamalkrishna, Majumdar, K. Majumder (Mrs.), and Lahiri S.C. "Studies on weak interactions : charge transfer and hydrogen bonding interactions of chloranil with substituted benzoic acids, amines and naphthols." Journal of Indian Chemical Society Vol. 79, Oct 2002 (2002): 811–14. https://doi.org/10.5281/zenodo.5847732.

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Department of Chemistry, F. C. College, Diamond Harbour, 24-Parganas(S), India Department of Chemistry, Barrackpore Rastraguru Surendra Nath College, 24-Parganas(N), India Department of Chemistry, University of Kalyani, Kalyani-741 235, India <em>Manuscript received 12 November 2001, revised 26 April 2002, accepted 14 May 2002</em> Stability constants for the charge transfer and hydrogen bonding interactions of chloranil with substituted benzoic acids, amines and naphthols have been determined in hydrogen-bonded solvent CHCl<sub>3</sub> and aprotic solvent C<sub>6</sub>H<sub>6</sub>. The chang

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7

ZHANG, YAN, CHANG-SHENG WANG та ZHONG-ZHI YANG. "ESTIMATION ON THE INTRAMOLECULAR 8- AND 12-MEMBERED RING N–H…O=C HYDROGEN BONDING ENERGIES IN β-PEPTIDES". Journal of Theoretical and Computational Chemistry 08, № 02 (2009): 279–97. http://dx.doi.org/10.1142/s0219633609004708.

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Computation of accurate hydrogen bonding energies in peptides is of great importance in understanding the conformational stabilities of peptides. In this paper, the intramolecular 8- and 12-membered ring N – H … O = C hydrogen bonding energies in β-peptide structures were evaluated. The optimal structures of the β-peptide conformers were obtained using MP2/6-31G(d) method. The MP2/6-311++G(d,p) calculations were then carried out to evaluate the single-point energies. The results show that the intramolecular 8-membered ring N – H … O = C hydrogen bonding energies in the five β-dipeptide structu

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8

Faust, Bruce C. "Hydrogen Bonding." Science 258, no. 5081 (1992): 381. http://dx.doi.org/10.1126/science.258.5081.381.c.

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9

Kollman, Peter A. "Hydrogen bonding." Current Biology 9, no. 14 (1999): R501. http://dx.doi.org/10.1016/s0960-9822(99)80319-4.

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10

Abraham, Michael H., Gary S. Whiting, Jenik Andonian-Haftvan, Jonathan W. Steed, and Jay W. Grate. "Hydrogen bonding." Journal of Chromatography A 588, no. 1-2 (1991): 361–0364. http://dx.doi.org/10.1016/0021-9673(91)85048-k.

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Дисертації з теми "Hydrogen bonding"

1

Mitchell, John Blayney Owen. "Theoretical studies of hydrogen bonding." Thesis, University of Cambridge, 1990. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.358697.

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2

Mondal, Raju. "Systematic studies of hydrogen bonding." Thesis, Durham University, 2004. http://etheses.dur.ac.uk/2986/.

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This thesis deals with wider application and implications of the hydrogen bond in crystal engineering studies and beyond; in addition, it also highlights the Cambridge Structural Database (CSD) as the potential knowledge-mine for inorganic chemists. The content of this thesis covers mainly three areas, viz, the role of hydrogen bonding in crystal engineering studies, the bridging between mainstream crystal engineering studies and solvates via hydrogen bond, and CSD studies on metal coordination spheres. Chapter 2 deals with crystal structure prediction through understanding the driving forces

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3

Sagar, Rajeeve. "Self-assembly via hydrogen bonding." Thesis, University of Warwick, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.247352.

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4

Scott, Tianeka S. "Understanding Hydrogen Bonding in Photoenolization." University of Cincinnati / OhioLINK, 2013. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1378196534.

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5

Howard, Daryl L., and n/a. "Hydrogen bonding in the near infrared." University of Otago. Department of Chemistry, 2006. http://adt.otago.ac.nz./public/adt-NZDU20060823.150321.

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OH-stretching spectra of various vapour phase species were recorded to investigate hydrogen bonding. The species studied include 1,2-ethanediol, 1,3-propanediol, 1,4-butanediol, acetylacetone, hexafluoroacetylacetone and the complex formed in the heterogeneous mixture of methanol and trimethylamine. The spectra range from the infrared, near infrared to visible wavelengths. The main focus of this study is in the near infrared region, in which the OH-stretching overtones are dominant. The near infrared and visible spectrum of formic acid has been recorded to investigate coupling across bonds,

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6

Biemond, Gerard Jan Eduard. "Hydrogen bonding in segmented block copolymers." Enschede : University of Twente, 2006. http://doc.utwente.nl/51102.

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7

Taylor, Russell Alan. "Hydrogen bonding effects in homogeneous catalysis." Thesis, Imperial College London, 2008. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.500138.

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8

Thomson, Patrick. "Extremely strong contiguous hydrogen bonding arrays." Thesis, University of Edinburgh, 2013. http://hdl.handle.net/1842/7856.

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When multiple hydrogen bonds lie in-plane and parallel to each other in close proximity, they experience additional positive or negative secondary electrostatic interactions. When a pair of molecules are arranged such that every hydrogen bond acceptor is on one molecule and every hydrogen bond donor is on another, the positive secondary electrostatic interactions are maximised, and thus the association constant of the complex is enhanced. This thesis will present the development of a family of quadruple hydrogen bonded complexes containing only positive secondary interactions, which confers un

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9

Locke, Christopher John. "Competitive hydrogen bonding in polymeric systems." Thesis, University of York, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.259805.

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10

Hayward, Owen David. "Hydrogen bonding in the crystalline state." Thesis, University of Bristol, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.391181.

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Книги з теми "Hydrogen bonding"

1

1941-, Schuster P., and Mikenda Werner, eds. Hydrogen bond research. Springer, 1999.

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2

1943-, Bellissent-Funel M. C., Dore John C, and NATO Advanced Research Workshop on Hydrogen Bond Networks (1993 : Cargèse, France), eds. Hydrogen bond networks. Kluwer Academic Publishers, 1994.

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3

D, Hadži, ed. Theoretical treatments of hydrogen bonding. John Wiley Sons, 1997.

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4

Kuo, Shiao-Wei. Hydrogen Bonding in Polymeric Materials. Wiley-VCH Verlag GmbH & Co. KGaA, 2018. http://dx.doi.org/10.1002/9783527804276.

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5

Jeffrey, George A., and Wolfram Saenger. Hydrogen Bonding in Biological Structures. Springer Berlin Heidelberg, 1991. http://dx.doi.org/10.1007/978-3-642-85135-3.

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6

Pihko, Petri M. Hydrogen Bonding in Organic Synthesis. WILEY-VCH, 2009.

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7

Jeffrey, George A. Hydrogen bonding in biological structures. Springer-Verlag, 1994.

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8

Wolfram, Saenger, ed. Hydrogen bonding in biological structures. Springer-Verlag, 1991.

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9

NATO Advanced Study Institute on Hydrogen-bonded Liquids (1989 Institut scientifique de Cargèse). Hydrogen-bonded liquids. Springer, 1991.

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10

NATO Advanced Study Institute on Hydrogen-bonded Liquids (1989 Institut scientifique de Cargèse). Hydrogen-bonded liquids. Kluwer Academic Publishers, 1991.

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Частини книг з теми "Hydrogen bonding"

1

Hirao, Hajime, and Xiaoqing Wang. "Hydrogen Bonding." In The Chemical Bond. Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527664658.ch17.

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2

Zhang, Chaoyang, Jing Huang, and Rupeng Bu. "Hydrogen Bonding, Hydrogen Transfer, and Halogen Bonding." In Intrinsic Structures and Properties of Energetic Materials. Springer Nature Singapore, 2023. http://dx.doi.org/10.1007/978-981-99-2699-2_9.

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3

Chen, Chang-Hwei. "Deuterium Bonding Versus Hydrogen Bonding." In Deuterium Oxide and Deuteration in Biosciences. Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-031-08605-2_3.

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4

Dong, Kun, Qian Wang, Xingmei Lu, Qing Zhou, and Suojiang Zhang. "Structure, Interaction and Hydrogen Bond." In Structure and Bonding. Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-38619-0_1.

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5

Huyskens, P. L., and G. G. Siegel. "Hydrogen Bonding and Entropy." In Intermolecular Forces. Springer Berlin Heidelberg, 1991. http://dx.doi.org/10.1007/978-3-642-76260-4_17.

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6

Vilar, Ramón. "Hydrogen-Bonding Templated Assemblies." In Supramolecular Assembly via Hydrogen Bonds II. Springer Berlin Heidelberg, 2004. http://dx.doi.org/10.1007/b14141.

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7

Todres, Zory Vlad. "Effects of Hydrogen Bonding." In Organic Chemistry in Confining Media. Springer International Publishing, 2013. http://dx.doi.org/10.1007/978-3-319-00158-6_4.

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8

Jeffrey, George A., and Wolfram Saenger. "Hydrogen Bonding in Carbohydrates." In Hydrogen Bonding in Biological Structures. Springer Berlin Heidelberg, 1994. http://dx.doi.org/10.1007/978-3-642-85135-3_13.

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9

Jeffrey, George A., and Wolfram Saenger. "Hydrogen Bonding in Proteins." In Hydrogen Bonding in Biological Structures. Springer Berlin Heidelberg, 1994. http://dx.doi.org/10.1007/978-3-642-85135-3_19.

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10

Hawthorne, F. C., and W. H. Baur. "Hydrogen Bonding in Minerals." In Advanced Mineralogy. Springer Berlin Heidelberg, 1994. http://dx.doi.org/10.1007/978-3-642-78523-8_23.

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Тези доповідей конференцій з теми "Hydrogen bonding"

1

Kasai, Paul H. "Hydrogen Bonding in Disk Lubricants." In 2006 Asia-Pacific Magnetic Recording Conference. IEEE, 2006. http://dx.doi.org/10.1109/apmrc.2006.365901.

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2

Dilshard, Rahima, John R. Dixon, William O. George, Robert A. Lewis, Brian Minty, and Roger Upton. "Molecular modeling of hydrogen bonding interactions." In Fourier Transform Spectroscopy: Ninth International Conference, edited by John E. Bertie and Hal Wieser. SPIE, 1994. http://dx.doi.org/10.1117/12.166742.

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3

Ilgen, Anastasia, Jeffery A. Greathouse, Ward Thompson, and Hasini Senanayake. "Hydrogen-bonding networks in nanoconfined water." In Goldschmidt2022. European Association of Geochemistry, 2022. http://dx.doi.org/10.46427/gold2022.9797.

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4

Ilgen, Anastasia, Jefferey Greathouse, Ward Thompson, and Hasini Senanayake. "Hydrogen-bonding networks in nanoconfined water." In Proposed for presentation at the Goldschmidt Meeting 2022 held July 10-15, 2022 in Honolulu, HI. US DOE, 2022. http://dx.doi.org/10.2172/2004088.

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5

Rusev, Rostislav. "Hydrogen bonding network as a logic gate." In 2017 XXVI International Scientific Conference "Electronics" (ET). IEEE, 2017. http://dx.doi.org/10.1109/et.2017.8124383.

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6

Pohl, Radek, Lenka Poštová Slavětínská, and Dominik Rejman. "Pyrrolidine nucleotides conformationally constrained via hydrogen bonding." In XVIth Symposium on Chemistry of Nucleic Acid Components. Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, 2014. http://dx.doi.org/10.1135/css201414352.

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7

Arrivo, S. M., T. P. Dougherty, W. T. Grubbs, and E. J. Heilweil. "New Advances in Measuring Hydrogen Bonding Dynamics." In International Conference on Ultrafast Phenomena. Optica Publishing Group, 1996. http://dx.doi.org/10.1364/up.1996.tha.3.

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We report the only known comprehensive study of conserved vibrational energy transfer during association and dissociation of biologically relevant hydrogen-bonded complexes in dilute (0.1 M acid) room temperature solution. Newly applied picosecond infrared techniques which vibrationally tag and probe interacting proton donating (-OH, -NH) and accepting (e.g., -C = O, ≡ON) constituents will be presented. From these measurements, details of steric interactions, equilibrium reaction rates and unexpected vibrational excitation transfer during hydrogen-bond formation are revealed for the first time

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8

McCoy, Anne, and Rachel Huchmala. "INSIGHTS INTO HYDROGEN BONDING FROM VIBRATIONAL SPECTRA." In 2023 International Symposium on Molecular Spectroscopy. University of Illinois at Urbana-Champaign, 2023. http://dx.doi.org/10.15278/isms.2023.6918.

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9

Nickel, Norbert H. "Hydrogen Bonding and Diffusion in Ti3C2 MXenes." In MATSUS Spring 2025 Conference. FUNDACIO DE LA COMUNITAT VALENCIANA SCITO, 2024. https://doi.org/10.29363/nanoge.matsusspring.2025.083.

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10

King, John, and Kevin Kubarych. "Solvent Dependent Spectral Diffusion in Hydrogen Bonding Environments." In International Conference on Ultrafast Phenomena. OSA, 2010. http://dx.doi.org/10.1364/up.2010.the17.

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Звіти організацій з теми "Hydrogen bonding"

1

Maroncelli, Mark. Ion Solvation and Hydrogen Bonding in Liquid Electrolytes. Office of Scientific and Technical Information (OSTI), 2023. http://dx.doi.org/10.2172/1970025.

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2

Zhou, Xu, Hunaid Nulwala, Hyung Kim, and Shiaoguo Chen. Universal Solvent Viscosity Reduction via Hydrogen Bonding Disruptors. Office of Scientific and Technical Information (OSTI), 2022. http://dx.doi.org/10.2172/1873907.

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3

Wendlandt, Johanna. Study of Hydrogen Bonding in Small Water Clusters with Density Functional Theory Calculations. Office of Scientific and Technical Information (OSTI), 2005. http://dx.doi.org/10.2172/877463.

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4

Roberds, B. E., K. D. Choquette, K. M. Geib, S. H. Kravitz, R. D. Twesten, and S. N. Farrens. Wafer bonding of GaAs, InP, and Si annealed without hydrogen for advanced device technologies. Office of Scientific and Technical Information (OSTI), 1997. http://dx.doi.org/10.2172/634098.

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5

Wei, Jing-Fong. Determination of the effect of various hydrogen bonding functionalities on the viscosity of coal liquids. Office of Scientific and Technical Information (OSTI), 1990. http://dx.doi.org/10.2172/6203549.

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6

Gragson, D. E., and G. L. Richmond. Investigations of the Structure and Hydrogen Bonding of Water Molecules at Liquid Surfaces by Vibrational Sum Frequency Spectroscopy. Defense Technical Information Center, 1998. http://dx.doi.org/10.21236/ada347409.

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7

Craven, S., D. Kramer, and W. Moddeman. Chemistry of glass-ceramic to metal bonding for header applications: 2. Hydrogen bubble formation during glass-ceramic to metal sealing. Office of Scientific and Technical Information (OSTI), 1986. http://dx.doi.org/10.2172/6963554.

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8

Gragson, D. E., and G. L. Richmond. Probing the Intermolecular Hydrogen Bonding of Water Molecules at the CCl sub 4 Water Interface in the Presence of Charged Soluble Surfactant. Defense Technical Information Center, 1998. http://dx.doi.org/10.21236/ada347139.

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9

Gao, Q., and J. C. Hemminger. A Vibrational Spectroscopy Study of CH3COOH, CH3COOD and (13)CD3COOH(D) Adsorption on Pt(111). 1. Surface Dimer Formation and Hydrogen Bonding. Defense Technical Information Center, 1991. http://dx.doi.org/10.21236/ada237240.

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10

Gao, Quanyin, and John C. Hemminger. A Vibrational Spectroscopy Study of Ch3COOH, CH3COOD and (13)CD3COOH(D) Adsorption on Pt (111): 1. Surface Dimer Formation and Hydrogen Bonding. Defense Technical Information Center, 1991. http://dx.doi.org/10.21236/ada237284.

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