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Journal articles on the topic 'Attochemistry of chemical bonding'

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Author: Grafiati

Published: 6 September 2023

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1

Bag, Sampad, Sankhabrata Chandra, Jayanta Ghosh, Anupam Bera, Elliot R. Bernstein, and Atanu Bhattacharya. "The attochemistry of chemical bonding." International Reviews in Physical Chemistry 40, no. 3 (July 3, 2021): 405–55. http://dx.doi.org/10.1080/0144235x.2021.1976499.

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2

BOERNER, LEIGH KRIETSCH. "CHEMICAL BONDING." Chemical & Engineering News 88, no. 42 (October 18, 2010): 39–41. http://dx.doi.org/10.1021/cen-v088n042.p039.

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3

Okino, Tomoya, Yusuke Furukawa, Yasuo Nabekawa, Shungo Miyabe, A. Amani Eilanlou, Eiji J. Takahashi, Kaoru Yamanouchi, and Katsumi Midorikawa. "Direct observation of an attosecond electron wave packet in a nitrogen molecule." Science Advances 1, no. 8 (September 2015): e1500356. http://dx.doi.org/10.1126/sciadv.1500356.

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Capturing electron motion in a molecule is the basis of understanding or steering chemical reactions. Nonlinear Fourier transform spectroscopy using an attosecond-pump/attosecond-probe technique is used to observe an attosecond electron wave packet in a nitrogen molecule in real time. The 500-as electronic motion between two bound electronic states in a nitrogen molecule is captured by measuring the fragment ions with the same kinetic energy generated in sequential two-photon dissociative ionization processes. The temporal evolution of electronic coherence originating from various electronic states is visualized via the fragment ions appearing after irradiation of the probe pulse. This observation of an attosecond molecular electron wave packet is a critical step in understanding coupled nuclear and electron motion in polyatomic and biological molecules to explore attochemistry.

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4

Senn, Peter. "On chemical bonding." American Journal of Physics 54, no. 7 (July 1986): 587. http://dx.doi.org/10.1119/1.14535.

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5

Putz, Mihai V. "Chemical action and chemical bonding." Journal of Molecular Structure: THEOCHEM 900, no. 1-3 (April 2009): 64–70. http://dx.doi.org/10.1016/j.theochem.2008.12.026.

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6

Balasubramanian, K. "Relativity and chemical bonding." Journal of Physical Chemistry 93, no. 18 (September 1989): 6585–96. http://dx.doi.org/10.1021/j100355a005.

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7

Ashcheulov, A. A., O. N. Manyk, T. O. Manyk, S. F. Marenkin, and V. R. Bilynskiy-Slotylo. "Chemical bonding in cadmium." Inorganic Materials 47, no. 9 (August 25, 2011): 952–56. http://dx.doi.org/10.1134/s0020168511090019.

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8

MORRISSEY, SUSAN R. "NSF'S CHEMICAL BONDING CENTERS." Chemical & Engineering News Archive 82, no. 41 (October 11, 2004): 33–34. http://dx.doi.org/10.1021/cen-v082n041.p033.

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9

JACOBY, MITCH. "CHEMICAL BONDING FORCES MEASURED." Chemical & Engineering News Archive 79, no. 14 (April 2, 2001): 12. http://dx.doi.org/10.1021/cen-v079n014.p012.

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10

Finzel, Kati. "Chemical bonding without orbitals." Computational and Theoretical Chemistry 1144 (November 2018): 50–55. http://dx.doi.org/10.1016/j.comptc.2018.10.004.

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11

Calais, Jean-Louis. "Chemical bonding and vibrations." Journal of Molecular Structure: THEOCHEM 261 (July 1992): 121–32. http://dx.doi.org/10.1016/0166-1280(92)87071-7.

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12

Jeung, G. H. "Chemical bonding in ScCS." Chemical Physics Letters 176, no. 2 (January 1991): 233–38. http://dx.doi.org/10.1016/0009-2614(91)90159-7.

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13

Zhao, Lili, Sudip Pan, Nicole Holzmann, Peter Schwerdtfeger, and Gernot Frenking. "Chemical Bonding and Bonding Models of Main-Group Compounds." Chemical Reviews 119, no. 14 (June 28, 2019): 8781–845. http://dx.doi.org/10.1021/acs.chemrev.8b00722.

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14

Cassiday, Laura. "The bonding of chemical giants." INFORM: International News on Fats, Oils, and Related Materials 27, no. 3 (March 1, 2016): 26–27. http://dx.doi.org/10.21748/inform.03.2016.26.

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15

Gonçalves, A. M., and Ana M. Segadães. "Unshaped Refractories with Chemical Bonding." Materials Science Forum 34-36 (January 1991): 705–9. http://dx.doi.org/10.4028/www.scientific.net/msf.34-36.705.

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16

Putz, Mihai. "Density Functionals of Chemical Bonding." International Journal of Molecular Sciences 9, no. 6 (June 26, 2008): 1050–95. http://dx.doi.org/10.3390/ijms9061050.

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17

Vaughan, D. J. "Chemical Bonding in Sulfide Minerals." Reviews in Mineralogy and Geochemistry 61, no. 1 (January 1, 2006): 231–64. http://dx.doi.org/10.2138/rmg.2006.61.5.

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18

Castro, Abril C., Mikael P. Johansson, Gabriel Merino, and Marcel Swart. "Chemical bonding in supermolecular flowers." Physical Chemistry Chemical Physics 14, no. 43 (2012): 14905. http://dx.doi.org/10.1039/c2cp42045g.

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19

Nishitani, Shigeto R., Shunsuke Fujii, Masataka Mizuno, Isao Tanaka, and Hirohiko Adachi. "Chemical bonding of3dtransition-metal disilicides." Physical Review B 58, no. 15 (October 15, 1998): 9741–45. http://dx.doi.org/10.1103/physrevb.58.9741.

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20

Lee, Chengteh, Han Chen, and George Fitzgerald. "Chemical bonding in water clusters." Journal of Chemical Physics 102, no. 3 (January 15, 1995): 1266–69. http://dx.doi.org/10.1063/1.468914.

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21

Sacks, Lawrence J. "Coulombic Models in Chemical Bonding." Journal of Chemical Education 77, no. 4 (April 2000): 445. http://dx.doi.org/10.1021/ed077p445.1.

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22

Marghussian, V. K., and R. Naghizadeh. "Chemical bonding of silicon carbide." Journal of the European Ceramic Society 19, no. 16 (December 1999): 2815–21. http://dx.doi.org/10.1016/s0955-2219(99)00068-0.

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23

Hagenmuller, Paul. "Intercalation chemistry and chemical bonding." Journal of Physics and Chemistry of Solids 59, no. 4 (April 1998): 503–6. http://dx.doi.org/10.1016/s0022-3697(97)90189-x.

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24

Harris, Mary. "Chemical Bonding Makes a Difference!" Journal of Chemical Education 83, no. 10 (October 2006): 1435. http://dx.doi.org/10.1021/ed083p1435.

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25

Hoffmann, P., O. Baake, B. Beckhoff, W. Ensinger, N. Fainer, A. Klein, M. Kosinova, et al. "Chemical bonding in carbonitride nanolayers." Nuclear Instruments and Methods in Physics Research Section A: Accelerators, Spectrometers, Detectors and Associated Equipment 575, no. 1-2 (May 2007): 78–84. http://dx.doi.org/10.1016/j.nima.2007.01.030.

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26

Harcourt, Richard D. "Kinetic energy and chemical bonding." American Journal of Physics 56, no. 7 (July 1988): 660–61. http://dx.doi.org/10.1119/1.15535.

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27

Hagenmuller, Paul. "Intercalation chemistry and chemical bonding." Journal of Power Sources 90, no. 1 (September 2000): 9–12. http://dx.doi.org/10.1016/s0378-7753(00)00437-7.

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28

Needham, Paul. "The source of chemical bonding." Studies in History and Philosophy of Science Part A 45 (March 2014): 1–13. http://dx.doi.org/10.1016/j.shpsa.2013.10.011.

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29

Greenspan, D. "Electron attraction and chemical bonding." Computers & Mathematics with Applications 38, no. 11-12 (December 1999): 217–27. http://dx.doi.org/10.1016/s0898-1221(99)00300-4.

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30

HAGENMULLER, P. "Chemical bonding and intercalation processes." Solid State Ionics 40-41 (August 1990): 3–9. http://dx.doi.org/10.1016/0167-2738(90)90275-v.

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31

Kematick, R. J., H. F. Franzen, and D. K. Misemer. "Chemical bonding interactions in Zr2Al." Journal of Solid State Chemistry 60, no. 3 (December 1985): 297–304. http://dx.doi.org/10.1016/0022-4596(85)90280-4.

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32

King, R. B. "Chemical bonding topology of superconductors." Journal of Solid State Chemistry 71, no. 1 (November 1987): 224–32. http://dx.doi.org/10.1016/0022-4596(87)90162-9.

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33

King, R. B. "Chemical bonding topology of superconductors." Journal of Solid State Chemistry 71, no. 1 (November 1987): 233–36. http://dx.doi.org/10.1016/0022-4596(87)90163-0.

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34

Weyrich, W. "Chemical bonding as electronic coherence." Acta Crystallographica Section A Foundations of Crystallography 58, s1 (August 6, 2002): c191. http://dx.doi.org/10.1107/s0108767302092668.

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35

Ghatikar, M. N. "Phase shifts and chemical bonding." Physica B: Condensed Matter 158, no. 1-3 (June 1989): 383–85. http://dx.doi.org/10.1016/0921-4526(89)90318-9.

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36

Cundari, Thomas R. "Chemical bonding involving d-orbitals." Chemical Communications 49, no. 83 (2013): 9521. http://dx.doi.org/10.1039/c3cc45204b.

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37

Batsanov, Stepan S. "Energy Electronegativity and Chemical Bonding." Molecules 27, no. 23 (November 25, 2022): 8215. http://dx.doi.org/10.3390/molecules27238215.

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Historical development of the concept of electronegativity (EN) and its significance and prospects for physical and structural chemistry are discussed. The current cutting-edge results are reviewed: new methods of determining the ENs of atoms in solid metals and of bond polarities and effective atomic charges in molecules and crystals. The ENs of nanosized elements are calculated for the first time, enabling us to understand their unusual reactivity, particularly the fixation of N2 by nanodiamond. Bond polarities in fluorides are also determined for the first time, taking into account the peculiarities of the fluorine atom’s electronic structure and its electron affinity.

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38

Herbst‐Irmer, Regine, and Erhard Irmer. "Experimental Visualisation of Chemical Bonding." CHEMKON 27, no. 6 (October 2020): 275–81. http://dx.doi.org/10.1002/ckon.202000015.

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39

King, R. B. "Chemical Bonding Topology of Superconductors." Journal of Solid State Chemistry 124, no. 2 (July 1996): 329–32. http://dx.doi.org/10.1006/jssc.1996.0245.

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40

King, R. B. "Chemical Bonding Topology of Superconductors." Journal of Solid State Chemistry 131, no. 2 (July 1997): 394–98. http://dx.doi.org/10.1006/jssc.1997.7415.

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41

Krapp, Andreas, F. Matthias Bickelhaupt, and Gernot Frenking. "Orbital Overlap and Chemical Bonding." Chemistry - A European Journal 12, no. 36 (December 13, 2006): 9196–216. http://dx.doi.org/10.1002/chem.200600564.

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42

Putz, Mihai V. "Chemical Bonding by the Chemical Orthogonal Space of Reactivity." International Journal of Molecular Sciences 22, no. 1 (December 28, 2020): 223. http://dx.doi.org/10.3390/ijms22010223.

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The fashionable Parr–Pearson (PP) atoms-in-molecule/bonding (AIM/AIB) approach for determining the exchanged charge necessary for acquiring an equalized electronegativity within a chemical bond is refined and generalized here by introducing the concepts of chemical power within the chemical orthogonal space (COS) in terms of electronegativity and chemical hardness. Electronegativity and chemical hardness are conceptually orthogonal, since there are opposite tendencies in bonding, i.e., reactivity vs. stability or the HOMO-LUMO middy level vs. the HOMO-LUMO interval (gap). Thus, atoms-in-molecule/bond electronegativity and chemical hardness are provided for in orthogonal space (COS), along with a generalized analytical expression of the exchanged electrons in bonding. Moreover, the present formalism surpasses the earlier Parr–Pearson limitation to the context of hetero-bonding molecules so as to also include the important case of covalent homo-bonding. The connections of the present COS analysis with PP formalism is analytically revealed, while a numerical illustration regarding the patterning and fragmentation of chemical benchmarking bondings is also presented and fundamental open questions are critically discussed.

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43

de Lange, Jurgens H., Daniël M. E. van Niekerk, and Ignacy Cukrowski. "Quantifying individual (anti)bonding molecular orbitals’ contributions to chemical bonding." Physical Chemistry Chemical Physics 21, no. 37 (2019): 20988–98. http://dx.doi.org/10.1039/c9cp04345d.

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44

Lusyana Yustin, Dessy, and Antuni Wiyarsi. "Students’ chemical literacy: A study in chemical bonding." Journal of Physics: Conference Series 1397 (December 2019): 012036. http://dx.doi.org/10.1088/1742-6596/1397/1/012036.

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45

WILKINSON, SOPHIE. "Gecko Bonding." Chemical & Engineering News 78, no. 24 (June 12, 2000): 14. http://dx.doi.org/10.1021/cen-v078n024.p014a.

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46

Shen, Yan-Fang, Chang Xu, and Long-Jiu Cheng. "Deciphering chemical bonding in BnHn2−(n = 2–17): flexible multicenter bonding." RSC Advances 7, no. 58 (2017): 36755–64. http://dx.doi.org/10.1039/c7ra06811e.

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47

Dereka, Bogdan, Qi Yu, Nicholas H. C. Lewis, William B. Carpenter, Joel M. Bowman, and Andrei Tokmakoff. "Crossover from hydrogen to chemical bonding." Science 371, no. 6525 (January 7, 2021): 160–64. http://dx.doi.org/10.1126/science.abe1951.

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Hydrogen bonds (H-bonds) can be interpreted as a classical electrostatic interaction or as a covalent chemical bond if the interaction is strong enough. As a result, short strong H-bonds exist at an intersection between qualitatively different bonding descriptions, with few experimental methods to understand this dichotomy. The [F-H-F]− ion represents a bare short H-bond, whose distinctive vibrational potential in water is revealed with femtosecond two-dimensional infrared spectroscopy. It shows the superharmonic behavior of the proton motion, which is strongly coupled to the donor-acceptor stretching and disappears on H-bond bending. In combination with high-level quantum-chemical calculations, we demonstrate a distinct crossover in spectroscopic properties from conventional to short strong H-bonds, which identify where hydrogen bonding ends and chemical bonding begins.

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48

Teterin, A. Yu, M. V. Ryzhkov, Yu A. Teterin, L. Vukčević, V. A. Terekhov, K. I. Maslakov, and K. E. Ivanov. "Nature of chemical bonding in ThF4." Radiochemistry 51, no. 6 (December 2009): 551–59. http://dx.doi.org/10.1134/s1066362209060010.

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49

Ashcheulov, A. A., O. N. Manik, and S. F. Marenkin. "Cadmium Antimonide: Chemical Bonding and Technology." Inorganic Materials 39 (2003): S59—S68. http://dx.doi.org/10.1023/b:inma.0000008886.21975.f8.

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50

Andreoni, Wanda, Paolo Giannozzi, and Michele Parrinello. "Molecular structure and chemical bonding inK3C60andK6C60." Physical Review B 51, no. 4 (January 15, 1995): 2087–97. http://dx.doi.org/10.1103/physrevb.51.2087.

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