Relevant bibliographies by topics / Metal nitride halides

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters
  4. Conference papers

Academic literature on the topic 'Metal nitride halides'

Author: Grafiati
Published: 4 June 2021
Last updated: 14 February 2022

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Journal articles on the topic "Metal nitride halides"

1

Fogg, Andrew M., Victoria M. Green, and Dermot O'Hare. "Superconducting intercalation compounds of metal nitride halides." Journal of Materials Chemistry 9, no. 7 (1999): 1547–51. http://dx.doi.org/10.1039/a809735f.

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2

Fuertes, Amparo. "Chemistry and superconductivity of intercalated metal nitride halides." Semiconductor Science and Technology 29, no. 6 (May 6, 2014): 064005. http://dx.doi.org/10.1088/0268-1242/29/6/064005.

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3

Li, Xiaofeng, Lin Xue, Lijuan Tang, and Ziyu Hu. "Pressure modulates the phase stability and physical properties of zinc nitride iodine." RSC Advances 5, no. 96 (2015): 78754–59. http://dx.doi.org/10.1039/c5ra14426d.

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To explore new stable phases in metal nitride halides, the structural, electronic and optical properties, and chemical bonding characteristics of Zn2NI under pressure were studied on the basis of crystal structure predicting evolution and density function calculations.
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4

Yamanaka, Shoji, Ken-ichi Hotehama, Takeshi Koiwasaki, Hitoshi Kawaji, Hiroshi Fukuoka, Shin-ichi Shamoto, and Tsuyoshi Kajitani. "Substitution and cointercalation effects on superconducting electron-doped layer structured metal nitride halides." Physica C: Superconductivity 341-348 (November 2000): 699–702. http://dx.doi.org/10.1016/s0921-4534(00)00654-7.

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5

Zhang, Xu, Zihe Zhang, Xudong Zhao, Dihua Wu, Xin Zhang, and Zhen Zhou. "Tetragonal-structured anisotropic 2D metal nitride monolayers and their halides with versatile promises in energy storage and conversion." Journal of Materials Chemistry A 5, no. 6 (2017): 2870–75. http://dx.doi.org/10.1039/c6ta10980b.

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6

Lulei, Michael. "Synthesis and Structure of CsNaLa6Br14N2and La3Br6N: Rare-Earth-Metal Nitride Halides with Isolated Bitetrahedral La6N2Units." Inorganic Chemistry 37, no. 4 (February 1998): 777–81. http://dx.doi.org/10.1021/ic9711269.

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7

Xu, Jie, Fei Wu, Quan Jiang, Jie-Kun Shang, and Yong-Xin Li. "Metal halides supported on mesoporous carbon nitride as efficient heterogeneous catalysts for the cycloaddition of CO2." Journal of Molecular Catalysis A: Chemical 403 (July 2015): 77–83. http://dx.doi.org/10.1016/j.molcata.2015.03.024.

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8

Liu, Xinyu, Shaoheng Yuan, Bin Xu, Xiaoning An, Jiahao Zhao, Jifang Li, and Lin Yi. "Ab initio prediction of thermoelectric performance of monolayer transition-metal nitride halides MNBr (M = Zr, Hf)." Journal of Physics and Chemistry of Solids 161 (February 2022): 110390. http://dx.doi.org/10.1016/j.jpcs.2021.110390.

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9

Kasahara, Yuichi, Kazuhiko Kuroki, Shoji Yamanaka, and Yasujiro Taguchi. "Unconventional superconductivity in electron-doped layered metal nitride halides MNX (M= Ti, Zr, Hf; X= Cl, Br, I)." Physica C: Superconductivity and its Applications 514 (July 2015): 354–67. http://dx.doi.org/10.1016/j.physc.2015.02.022.

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10

LULEI, M. "ChemInform Abstract: Synthesis and Structure of CsNaLa6Br14N2 and La3Br6N: Rare-Earth-Metal Nitride Halides with Isolated Bitetrahedral La6N2 Units." ChemInform 29, no. 20 (June 22, 2010): no. http://dx.doi.org/10.1002/chin.199820003.

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Dissertations / Theses on the topic "Metal nitride halides"

1

Fogg, Andrew Michael. "Structural, kinetic and synthetic studies of intercalation compounds." Thesis, University of Oxford, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.297906.

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Fauxpoint, Didier. "Polymeres en peigne mesomorphes a caractere electroactif obtenus par polymerisation cationique de mesogenes polaires." Clermont-Ferrand 2, 1988. http://www.theses.fr/1988CLF21071.

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Elaboration et etude de polymeres a chaine conjuguees possedant une structure en peigne:(rc=n)::(n). Les monomeres synthetises ont une architecture chimique analogue a celle des mesogenes thermotropes classiques. Le decouplage du groupe polymerisable(cn) par rapport au "coeur aromatique" de la molecule leur confere un caractere original. La synthese du polymere necessite la complexation du monomere avec un halogenure de metal de transition. Le caractere electroactif du polymere est etudie par dopage en phase cristalline
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Book chapters on the topic "Metal nitride halides"

1

Suginome, M., and Y. Ito. "Nucleophilic Substitution of Halides with Metal Cyanides." In Three Carbon-Heteroatom Bonds: Nitriles, Isocyanides, and Derivatives, 1. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-019-00311.

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2

Taber, Douglass F. "Substituted Benzenes: The Li Synthesis of Rubriflordilactone A." In Organic Synthesis. Oxford University Press, 2017. http://dx.doi.org/10.1093/oso/9780190646165.003.0063.

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Cheol-Hong Cheon of Korea University (J. Org. Chem. 2014, 79, 7277) and Toshiyuki Kamei and Toyoshi Shimada of the Nara National College of Technology (Tetrahedron Lett. 2014, 55, 4245) described the ring bromination of arene boronates. The boronate can then be removed, enabling the conversion of 1 to 2. Yu Rao of Tsinghua University constructed (Chem. Commun. 2014, 50, 15037) the sulfone 5 by coupling the arenes 3 and 4 with K2S2O8. Igor Larrosa of Queen Mary University of London assembled (Chem. Sci. 2014, 5, 3509) the biphenyl 8 by arylating 6 with the iodide 7. Guy Bertrand of the University of California, San Diego showed (J. Am. Chem. Soc. 2014, 136, 13594) that under Au catalysis, the aniline 9 was sufficiently nucleophilic to add in a conjugate sense to the enone 10 to give 11. Hideo Togo of Chiba University optimized (Eur. J. Org. Chem. 2014, 6077) condi­tions for the selective ortho formylation of a phenol 12. The crude reaction mixture could also be directly oxidized with I2/ NH3 to give the nitrile 13. Silas P. Cook of Indiana University ortho metalated (J. Am. Chem. Soc. 2014, 136, 13130; Angew. Chem. Int. Ed. 2014, 53, 11065) the benzamide 14, then used an iron catalyst to couple that intermediate with a halide 15, leading to the alkylated product 16. As with the phenol 12 and the benzamide 14, aromatic functionalization has usu­ally been directed by a functional group directly attached to the ring. Daqin Shi and Yingsheng Zhao of Soochow University showed (Chem. Sci. 2014, 5, 4962) that a longer tether can be effective, as illustrated by the conversion of 17 to 19. Debabrata Maiti of the Indian Institute of Technology Bombay also used (Org. Lett. 2014, 16, 5760) a longer tether for the selective meta functionalization of 20 to 22. Motohiro Sonoda of Osaka Prefecture University constructed (Tetrahedron Lett. 2014, 55, 5302) the phenol 25 by acid-mediated rearrangement of the Diels–Alder adduct of 24 with the furan 23. Anthony G. M. Barrett of Imperial College London devised (J. Org. Chem. 2014, 79, 8706) conditions for the iodinative cyclization of 26 to 27.
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Conference papers on the topic "Metal nitride halides"

1

Cegielski, P. J., S. Neutzner, C. Porschatis, M. Gandini, D. Schall, C. A. R. Perini, J. Bolten, et al. "Efficient Metal-Halide Perovskite Micro Disc Lasers Integrated in a Silicon Nitride Photonic Platform." In 2018 76th Device Research Conference (DRC). IEEE, 2018. http://dx.doi.org/10.1109/drc.2018.8442221.

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Journal articles
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