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Journal articles on the topic 'Heteroatomic1'

Author: Grafiati

Published: 6 September 2023

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1

Lin, Jin-Yi, Bin Liu, Meng-Na Yu, et al. "Understanding the molecular gelation processes of heteroatomic conjugated polymers for stable blue polymer light-emitting diodes." Journal of Materials Chemistry C 5, no. 27 (2017): 6762–70. http://dx.doi.org/10.1039/c7tc01541k.

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2

Ovchinnikov, V. V., L. R. Khazieva, L. I. Lapteva, and A. I. Konovalov. "Thermochemistry of heteroatomic compounds." Russian Chemical Bulletin 49, no. 1 (1990): 33–38. http://dx.doi.org/10.1007/bf02499061.

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3

Ovchinnikov, V. V., T. B. Makeeva, L. I. Lapteva, V. A. Valiullina, L. M. Pilishkina, and A. I. Konovalov. "Thermochemistry of heteroatomic compounds." Journal of Thermal Analysis 45, no. 4 (1995): 735–39. http://dx.doi.org/10.1007/bf02548889.

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4

Ovchinnikov, V. V., L. I. Lapteva, E. Yu Sitnikova, and A. I. Konovalov. "Thermochemistry of heteroatomic compounds." Russian Chemical Bulletin 49, no. 9 (2000): 1522–25. http://dx.doi.org/10.1007/bf02495153.

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5

Ovchinnikov, V. V., L. I. Lapteva, and M. G. Kireev. "Thermochemistry of heteroatomic compounds." Russian Chemical Bulletin 53, no. 8 (2004): 1761–62. http://dx.doi.org/10.1007/s11172-005-0031-z.

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6

Zhang, Kai, Benjamin B. Noble, Adam C. Mater, Michael J. Monteiro, Michelle L. Coote, and Zhongfan Jia. "Effect of heteroatom and functionality substitution on the oxidation potential of cyclic nitroxide radicals: role of electrostatics in electrochemistry." Physical Chemistry Chemical Physics 20, no. 4 (2018): 2606–14. http://dx.doi.org/10.1039/c7cp07444a.

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7

Roy, Matthew M. D., Michael J. Ferguson, Robert McDonald, Yuqiao Zhou, and Eric Rivard. "A vinyl silylsilylene and its activation of strong homo- and heteroatomic bonds." Chemical Science 10, no. 26 (2019): 6476–81. http://dx.doi.org/10.1039/c9sc01192g.

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8

Lv, Jing-Hui, Xian-Yong Wei, Ying-Hua Wang, et al. "Characterization of condensed aromatics and heteroatomic species in Yanshan petroleum coke through ruthenium ion-catalyzed oxidation using three mass spectrometers." RSC Advances 6, no. 66 (2016): 61758–70. http://dx.doi.org/10.1039/c6ra09194f.

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9

Chen, Jiazhi, Fang Lu, and Jie Xu. "Formation of uniform hollow nanocages with heteroatom-doped MCM-41 structures." RSC Advances 5, no. 7 (2015): 5068–71. http://dx.doi.org/10.1039/c4ra13959c.

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10

Li, Caixia, Shihua Dong, Rui Tang, et al. "Heteroatomic interface engineering in MOF-derived carbon heterostructures with built-in electric-field effects for high performance Al-ion batteries." Energy & Environmental Science 11, no. 11 (2018): 3201–11. http://dx.doi.org/10.1039/c8ee01046c.

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11

Reuter, K., R. G. M. Maas, A. Reuter, F. Kilgenstein, Y. Asfaha, and C. von Hänisch. "Synthesis of heteroatomic bridged paracyclophanes." Dalton Transactions 46, no. 14 (2017): 4530–41. http://dx.doi.org/10.1039/c7dt00321h.

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Heteroatomic bridged paracyclophanes with Si<sub>2</sub>N, Si<sub>2</sub>P, Si<sub>2</sub>(NGa)<sub>2</sub>and Si<sub>2</sub>(PGa)<sub>2</sub>linkers were accessed by diverse synthetic approaches and were characterised among others by X-ray diffraction.

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12

Tomio, L., M. T. Yamashita, T. Frederico, and F. Bringas. "Borromean three-body heteroatomic resonances." Laser Physics 21, no. 8 (2011): 1464–69. http://dx.doi.org/10.1134/s1054660x11150229.

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13

Korch, Katerina M., and Donald A. Watson. "Cross-Coupling of Heteroatomic Electrophiles." Chemical Reviews 119, no. 13 (2019): 8192–228. http://dx.doi.org/10.1021/acs.chemrev.8b00628.

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14

Laitinen, Risto S., Pentti Pekonen, and Reijo J. Suontamo. "Homo- and heteroatomic chalcogen rings." Coordination Chemistry Reviews 130, no. 1-2 (1994): 1–62. http://dx.doi.org/10.1016/0010-8545(94)80002-2.

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15

Sun, Fugen, Bo Zhang, Hao Tang, et al. "Heteroatomic TexS1−x molecule/C nanocomposites as stable cathode materials in carbonate-based electrolytes for lithium–chalcogen batteries." Journal of Materials Chemistry A 6, no. 21 (2018): 10104–10. http://dx.doi.org/10.1039/c8ta02751j.

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16

Wang, Peng, Xuelin Shi, Chunhong Fu, et al. "Strong pyrrolic-N–Pd interactions boost the electrocatalytic hydrodechlorination reaction on palladium nanoparticles." Nanoscale 12, no. 2 (2020): 843–50. http://dx.doi.org/10.1039/c9nr07528c.

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We demonstrated that heteroatomic nitrogen (N) doping of graphene can significantly enhance the performance of the graphene–palladium nanoparticle composite catalyst (N/G-Pd) in the electrocatalytic hydrodechlorination (EHDC) reaction.

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17

Huang, Liping, Wenyao Li, Xudun Shen, et al. "Phosphorus-bridged ternary metal alloy encapsulated in few-layered nitrogen-doped graphene for highly efficient electrocatalytic hydrogen evolution." Journal of Materials Chemistry A 10, no. 13 (2022): 7111–21. http://dx.doi.org/10.1039/d1ta10032g.

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A strategy of improving the stability and tuning the activity of transition metal catalysts via nitrogen-doped graphene encapsulation and heteroatomic doping is elaborated here. This work makes for achieving precise regulation of electrocatalysts.

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18

Bhalothia, Dinesh, Po-Chun Chen, Che Yan, et al. "Heterogeneous assembly of Pt-clusters on hierarchically structured CoOx@SnPd2@SnO2 quaternary nanocatalysts manifesting oxygen reduction reaction performance." New Journal of Chemistry 44, no. 23 (2020): 9712–24. http://dx.doi.org/10.1039/d0nj01154a.

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Atomic Pt clusters in the heterogeneous interface of CoO<sub>x</sub>@SnPd<sub>2</sub>@SnO<sub>2</sub> possess high heteroatomic intermixing facilities, oxygen splitting and hydration reactions resulting in high performance ORR.

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19

Meng, Yiming, Juan An, Lei Chen, et al. "A NaNi0.5Mn0.5SnxO2 cathode with anti-structural deformation enhancing long lifespan and super power for a sodium ion battery." Chemical Communications 56, no. 58 (2020): 8079–82. http://dx.doi.org/10.1039/d0cc02168g.

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Introduction of Sn<sup>4+</sup> enlarges the interlayer spacing and builds a heteroatomic skeleton preventing multiphase transition of O3-NaNi<sub>0.5</sub>Mn<sub>0.5</sub>O<sub>2</sub> for a sodium ion battery.

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20

Li, Guifang, Yawen Li, Jingxia Deng, Huiting Lin, Xinyi Hou, and Lishan Jia. "Ultrahigh rate capability supercapacitors based on tremella-like nitrogen and phosphorus co-doped graphene." Materials Chemistry Frontiers 4, no. 9 (2020): 2704–15. http://dx.doi.org/10.1039/d0qm00392a.

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The incorporation of heteroatomic atoms into the graphene crystal lattice not only effectively introduces the bandgap but also increases the defects and the localized reactivity of the graphene, and thereby the remarkable electrochemical properties of graphene are imparted.

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21

Zwanenburg, B. "Synthetic potential of heteroatomic ring systems." Pure and Applied Chemistry 71, no. 3 (1999): 423–30. http://dx.doi.org/10.1351/pac199971030423.

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22

Vulovic, Bojan, and Donald A. Watson. "Heck-Like Reactions Involving Heteroatomic Electrophiles." European Journal of Organic Chemistry 2017, no. 34 (2017): 4996–5009. http://dx.doi.org/10.1002/ejoc.201700485.

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23

Li, Da-Zhi, Li-Juan Zhang, Ting Ou, et al. "Ternary B2X2H2(X = O and S) rhombic clusters and their potential use as inorganic ligands in sandwich-type (B2X2H2)2Ni complexes." Physical Chemistry Chemical Physics 17, no. 26 (2015): 16798–804. http://dx.doi.org/10.1039/c5cp02394g.

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Boron-based ternary B<sub>2</sub>O<sub>2</sub>H<sub>2</sub>and B<sub>2</sub>S<sub>2</sub>H<sub>2</sub>clusters possess a rhombic, heteroatomic ring with 4π electrons in a nonbonding/bonding combination, differing from cyclobutadiene.

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24

Maitte, Pierre, Marie-Claude Bellassoud-Fargeau, Bernadette Graffe, and Marie-Claude Sacquet. "Synthesis of Novel N-Heteroatomic Cannabinol Analogues." HETEROCYCLES 24, no. 10 (1986): 2831. http://dx.doi.org/10.3987/r-1986-10-2831.

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25

Rao, B. K., and P. Jena. "Electronic structure and geometries of heteroatomic clusters." Physical Review B 37, no. 6 (1988): 2867–73. http://dx.doi.org/10.1103/physrevb.37.2867.

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26

Zong, Jie, Joel T. Mague, E. Celeste Welch, Isaac M. K. Eckert, and Robert A. Pascal. "Sterically congested macrobicycles with heteroatomic bridgehead functionality." Tetrahedron 69, no. 48 (2013): 10316–21. http://dx.doi.org/10.1016/j.tet.2013.10.018.

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27

Zupancic, Joseph J., Peter B. Grasse, Stephen C. Lapin, and Gary B. Schuster. "The reactions of fluorenylidene with heteroatomic nucleophiles." Tetrahedron 41, no. 8 (1985): 1471–78. http://dx.doi.org/10.1016/s0040-4020(01)96388-4.

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28

Vignolini, Silvia, Francesca Intonti, Francesco Riboli, et al. "Ideal homoatomic and heteroatomic photonic crystal molecules." Photonics and Nanostructures - Fundamentals and Applications 10, no. 3 (2012): 271–75. http://dx.doi.org/10.1016/j.photonics.2011.05.001.

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29

Litinskii, G. B., and V. E. Krikunova. "FRee electron model for heteroatomic conjugate molecules." Journal of Structural Chemistry 50, no. 6 (2009): 1029–34. http://dx.doi.org/10.1007/s10947-009-0152-6.

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30

Griffiths, J. "Diazo chemistry I: Aromatic and heteroatomic compounds." Dyes and Pigments 27, no. 3 (1995): 261–62. http://dx.doi.org/10.1016/0143-7208(95)90005-5.

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31

LAITINEN, R. S., P. PEKONEN, and R. J. SUONTAMO. "ChemInform Abstract: Homo- and Heteroatomic Chalcogen Rings." ChemInform 25, no. 23 (2010): no. http://dx.doi.org/10.1002/chin.199423288.

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32

Li, Da-Zhi, Lin-Yan Feng, Ling Pei, Li-Juan Zhang, Shu-Guo Wu та Hua-Jin Zhai. "Pentagonal five-center four-electron π bond in ternary B3N2H5 cluster: an extension of the concept of three-center four-electron ω bond". Physical Chemistry Chemical Physics 19, № 3 (2017): 2479–86. http://dx.doi.org/10.1039/c6cp07954g.

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Ternary B<sub>3</sub>N<sub>2</sub>H<sub>5</sub> (C<sub>2v</sub>, <sup>1</sup>A<sub>1</sub>) cluster has a heteroatomic B<sub>3</sub>N<sub>2</sub> ring, with 4π electrons in a robust bonding/nonbonding combination, which is proposed as a five-center four-electron o-bond.

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33

Mitzinger, Stefan, Jascha Bandemehr, Kevin Reiter, et al. "(Ge2P2)2−: a binary analogue of P4 as a precursor to the ternary cluster anion [Cd3(Ge3P)3]3−." Chemical Communications 54, no. 12 (2018): 1421–24. http://dx.doi.org/10.1039/c7cc08348c.

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The novel binary P<sub>4</sub> analogue (Ge<sub>2</sub>P<sub>2</sub>)<sup>2−</sup> proved to be a suitable precursor for heteroatomic cluster synthesis. Upon reaction with CdPh<sub>2</sub>, an unprecedented cluster anion is formed, [Cd<sub>3</sub>(Ge<sub>3</sub>P)<sub>3</sub>]<sup>−</sup>.

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34

Mukhin, Nikolay V., and Mykhailo M. Kutia. "Thiophene Determination in Liquid Hydrocarbons by In-line Acoustic Measurements." Journal of the Russian Universities. Radioelectronics 22, no. 4 (2019): 82–88. http://dx.doi.org/10.32603/1993-8985-2019-22-4-82-88.

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Introduction. Petroleum is a complex mixture of hydrocarbons. Sulphur is the most common heteroatom in pe-troleum and petroleum products. Its content in oil can reach 14 %. The determination of sulphur in oil and its removal is of great importance, since sulphur compounds adversely affect the quality of petroleum products and pollute the environment. Desulphurization of hydrocarbons is important in the processing of petroleum products, which needs in usage of accurate and simple methods for the sulphur-containing components determination. Most of developed methods are difficult to apply for fl

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35

Dufresne, Stéphane, Thomas Skalski, and W. G. Skene. "Insights into the effect of ketylimine, aldimine, and vinylene group attachment and regiosubstitution on the fluorescence deactivation of fluorene." Canadian Journal of Chemistry 89, no. 2 (2011): 173–80. http://dx.doi.org/10.1139/v10-089.

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The spectroscopic and electrochemical properties of a 9-substituted fluorene ketylimine (3) were investigated and compared with those of its vinylene analogue (4) to determine the origins of the quenched fluorescence of these compounds. The predominate mode of singlet excited state deactivation of the heteroatomic fluorene was found to be internal conversion involving bond rotation. Meanwhile, its carbon counterpart was found to undergo deactivation preferentially by intersystem crossing to form its triplet, which was confirmed by laser flash photolysis. Both 3 and 4 quenched the fluorescence

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36

Chen, Xiao-Bo, Xin-Yang Zhang, Ru-Meng Qin, et al. "Distribution of nitrogen and oxygen compounds in shale oil distillates and their catalytic cracking performance." Petroleum Science 17, no. 6 (2020): 1764–78. http://dx.doi.org/10.1007/s12182-020-00508-z.

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AbstractThe positive- and negative-ion electrospray ionization (ESI) coupled with Fourier transform-ion cyclotron resonance mass spectrometry (FT-ICR MS) was employed to identify the chemical composition of heteroatomic compounds in four distillates of Fushun shale oil, and their catalytic cracking performance was investigated. There are nine classes of basic nitrogen compounds (BNCs) and eleven classes of non-basic heteroatomic compounds (NBHCs) in the different distillates. The dominant BNCs are mainly basic N1 class species. The dominant NBHCs are mainly acidic O2 and O1 class species in th

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37

Xian-Mei, MENG, HUANG Xiao-Ming, and WANG Chuan-Kui. "Two-photon Absorption Properties of Heteroatomic Ring Molecules." Acta Physico-Chimica Sinica 23, no. 02 (2007): 228–31. http://dx.doi.org/10.3866/pku.whxb20070217.

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38

Gal'pern, Elena G., Vladimir V. Pinyaskin, Ivan V. Stankevich, and Leonid A. Chernozatonskii. "Heteroatomic Nanotubes with Quasi-One-Dimensional Superlattice Structure." Journal of Physical Chemistry B 101, no. 5 (1997): 705–9. http://dx.doi.org/10.1021/jp961669o.

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39

Lermontov, Sergei. "Book Review, Ligand Coupling Reactions with Heteroatomic Compounds." Synthesis 2000, no. 04 (2000): 609–10. http://dx.doi.org/10.1055/s-2000-6356.

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40

Golushkova, E. B., Alexander P. Ilyin, and A. V. Mostovshchikov. "Extraction of Oil Heteroatomic Compounds Using Metal Powders." Key Engineering Materials 685 (February 2016): 743–47. http://dx.doi.org/10.4028/www.scientific.net/kem.685.743.

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The paper presents results of scanning electron microscope (SEM) investigations, differential thermal and elemental analyses, and infrared (IR) spectroscopy of micron powders obtained by thermal decomposition of cupric and nickel oxalates before and after their blending with oil. The oil treatment modifies the powder compositions, heteroorganic compounds extracted from oil are observed on their surface. The analysis shows that materials based on copper and nickel micron powders can be used for the prepurification of crude hydrocarbons from heteroatomic compounds.

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41

Levin, A. A. "Heteroatomic molecules and heteroligand complexes within perturbation theory." Journal of Structural Chemistry 29, no. 6 (1989): 828–36. http://dx.doi.org/10.1007/bf00748424.

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42

Sharma, Pooja. "Spectroscopic analysis of Jet A-1 heteroatomic components." Chemical Engineering Science 207 (November 2019): 588–99. http://dx.doi.org/10.1016/j.ces.2019.06.059.

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43

Zwanenburg, Binne. "ChemInform Abstract: Synthetic Potential of Heteroatomic Ring Systems." ChemInform 30, no. 52 (2010): no. http://dx.doi.org/10.1002/chin.199952279.

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44

Daoust, Benoit, Nicolas Gilbert, Paméla Casault, François Ladouceur, and Simon Ricard. "1,2-Dihaloalkenes in Metal-Catalyzed Reactions." Synthesis 50, no. 16 (2018): 3087–113. http://dx.doi.org/10.1055/s-0037-1610174.

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1,2-Dihaloalkenes readily undergo simultaneous or sequential difunctionalization through transition-metal-catalyzed reactions, which makes them attractive building blocks for complex unsaturated motifs. This review summarizes recent applications of such transformations in C–C and C–heteroatom bond forming processes. The facile synthesis of stereodefined alkene derivatives, as well as aromatic and heteroatomic compounds, from 1,2-dihaloalkenes is thus outlined.1 Introduction2 Synthesis of 1,2-Dihaloalkenes3 C–C Bond Forming Reactions4 C–Heteroatom Bond Forming Reactions5 Conclusion

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45

Cheng, Xiong, and Dujie Hou. "Characterization of Severely Biodegraded Crude Oils Using Negative-Ion ESI Orbitrap MS, GC-NCD and GC-SCD: Insights into Heteroatomic Compounds Biodegradation." Energies 14, no. 2 (2021): 300. http://dx.doi.org/10.3390/en14020300.

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A slightly and two severely biodegraded crude oils with the same origin were analysed using negative-ion electrospray ionization Orbitrap mass spectrometry (ESI Orbitrap MS), gas chromatography-nitrogen chemiluminescence detector (GC-NCD), and GC-sulfur chemiluminescence detector (GC-SCD) to investigate the composition of heteroatomic compounds and their fate during severe biodegradation and to provide insights into biodegradation pathway of hopanes, nitrogen- and sulfur-containing compounds. Twelve heteroatomic compound classes, including O1–O5, N1, N2, N1O1–N1O3, N1S1 and O3S1, were detected

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46

Cheng, Xiong, and Dujie Hou. "Characterization of Severely Biodegraded Crude Oils Using Negative-Ion ESI Orbitrap MS, GC-NCD and GC-SCD: Insights into Heteroatomic Compounds Biodegradation." Energies 14, no. 2 (2021): 300. http://dx.doi.org/10.3390/en14020300.

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A slightly and two severely biodegraded crude oils with the same origin were analysed using negative-ion electrospray ionization Orbitrap mass spectrometry (ESI Orbitrap MS), gas chromatography-nitrogen chemiluminescence detector (GC-NCD), and GC-sulfur chemiluminescence detector (GC-SCD) to investigate the composition of heteroatomic compounds and their fate during severe biodegradation and to provide insights into biodegradation pathway of hopanes, nitrogen- and sulfur-containing compounds. Twelve heteroatomic compound classes, including O1–O5, N1, N2, N1O1–N1O3, N1S1 and O3S1, were detected

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47

Zhang, Lei, Caiyi Lu, and Yingcai Long. "Synthesis, characterization of an AlPO-CJ2analogue containing heteroatomic Eu." Chem. Commun., no. 18 (2002): 2064–65. http://dx.doi.org/10.1039/b205254g.

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48

Scheit, Simona, Vitali Averbukh, Hans-Dieter Meyer, Jürgen Zobeley, and Lorenz S. Cederbaum. "Interatomic Coulombic decay in a heteroatomic rare gas cluster." Journal of Chemical Physics 124, no. 15 (2006): 154305. http://dx.doi.org/10.1063/1.2185637.

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49

Grineva, O. V. "Intermolecular halogen...halogen contacts in crystals with heteroatomic halogens." Acta Crystallographica Section A Foundations of Crystallography 68, a1 (2012): s67. http://dx.doi.org/10.1107/s0108767312098716.

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50

Labbe, Nicole J., Vikram Seshadri, Tina Kasper, Nils Hansen, Patrick Oßwald, and Phillip R. Westmoreland. "Flame chemistry of tetrahydropyran as a model heteroatomic biofuel." Proceedings of the Combustion Institute 34, no. 1 (2013): 259–67. http://dx.doi.org/10.1016/j.proci.2012.07.027.

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