Relevant bibliographies by topics / Bromo complex

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

Academic literature on the topic 'Bromo complex'

Author: Grafiati
Published: 4 June 2021
Last updated: 2 February 2022

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Journal articles on the topic "Bromo complex"

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Chan, Lisa M., Atta M. Arif та Richard D. Ernst. "Solid State Structure of Bis[(bromo)(dicyclopentadienyl)vanadium(μ2-fluoro)][(bromo)(cyclopentadienyl)vanadium][tetrafluoroborate]". Journal of Crystallography 2015 (29 листопада 2015): 1–4. http://dx.doi.org/10.1155/2015/312963.

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The new complex [V(C5H5)2Br]2(μ2-F)2[V(C5H5)Br]+[BF4]− has been isolated from the reaction of vanadocene monobromide with the ferrocenium cation. The complex is a mixed valence compound composed of two V(IV) and one V(III) centers. The V(III) center has one cyclopentadienyl ligand in its coordination sphere, as well as a bromide and two fluoride ligands. Each fluoride ligand is also attached to one of the V(IV) centers, which additionally is coordinated by a bromide and two cyclopentadienyl ligands. The complex crystallizes in the monoclinic space group P21/m, with a=7.66490(10) Å, b=15.2457(2
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Gingl, Franz, та Joachim Strähle. "Synthese und Struktur von μ-Bromo-μ-dioxo-bis( phthalocyaninato-niob(V))tribromid, [(PcNb)2O2Br]+Br3-, einem zweikernigen Phthalocyaninatokomplex / Synthesis and Structure of μ-Bromo-μ-dioxo-bis(phthalocyaninato-niobium(V))tribromide, [(PcNb)2O2Br]+Br3-, a Dinuclear Phthalocyaninato Complex". Zeitschrift für Naturforschung B 44, № 2 (1989): 110–16. http://dx.doi.org/10.1515/znb-1989-0202.

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Abstract dioxo-bis(phthaIocyaninato-niob(V))tribromid, [(PcNb)20 2Br]+BrJ, einem zweikernigen Phthalocyaninatokomplex Synthesis and Structure of i w-Bromo-/ i/-dioxo-bis(phthalocyaninato-niobium(V))tribromide, [(PcNb)20 2Br]~Br3 , i w -Brom o-^-dioxo-bis(phthalocyaninato-niobium (V))tribrom ide. Synthesis. Crystal Structure
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Corredoira-Vázquez, Julio, Matilde Fondo, Jesús Sanmartín-Matalobos, and Ana M. García-Deibe. "2D Supramolecular Structure for a Chiral Heterotrinuclear ZnII2HoIII Complex through Varied HBonds Connecting Solvates and Counterions." Proceedings 2, no. 14 (2018): 1114. http://dx.doi.org/10.3390/iecc_2018-05247.

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We report the crystal structure of [ZnII2HoIII(L)(ald)(HO)(H2O)3(MeCN)](NO3)2·EtOH [H3L = 2-(5-bromo-2-hydroxy-3-methoxyphenyl)-1,3-bis[4-(5-bromo-2-hydroxy-3-methoxyphenyl)-3-azabut-3-enyl]-1,3-imidazolidine) and Hald = 5-bromo-2-hydroxy-3-methoxy-benzaldehyde]. Despite the presence of two bulky multidentate ligands, as well as several monodentate ligands surrounding the nonacoordinate holmium cation, and the two pseudooctahedral zinc ions, the intricate H-bonded system formed by this chiral heterotrinuclear complex is only expanded in a 2D supramolecular structure. The interactions involve t
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Lashgari, A., and Sh Ghammamy. "Synthesis and characterization of new bromomolybdate complex (C6H13)4N MoO3Br." Bangladesh Journal of Scientific and Industrial Research 50, no. 4 (2015): 297–99. http://dx.doi.org/10.3329/bjsir.v50i4.25840.

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The reaction between tetrahexylammonium bromide and MoO3 produced a new bromo salt (bromotrioxomolybdate (VI)). (C6H13)4N [MoO3Br], characterized by IR, UV/Visible and 81Br-NMR techniques.Bangladesh J. Sci. Ind. Res. 50(4), 297-299, 2015
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Toda, Miura, Miya та Takenaka. "Synthesis of Brominated Polyethylene by Copolymerization of Ethylene with ω–bromoalkene Catalyzed by a Metallocene and Methylaluminoxane System". Catalysts 9, № 8 (2019): 660. http://dx.doi.org/10.3390/catal9080660.

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The metallocene-catalyzed copolymerization of ethylene and 11–bromo–1–undecene was carried out to synthesize brominated polyethylene (PE). A modified methylaluminoxane (MMAO) solution was used as a cocatalyst and rac–Et(H4Ind)2ZrCl2 as a catalyst. The copolymerization showed a high activity and afforded the copolymer with a 11-bromo-1-undecene incorporation ranging from 1.0 to 4.3 mol%. When using a dried methylaluminoxane (dMAO) as a cocatalyst, the incorporation ratio of 11-bromo-1-undecene increased remarkably to 25.2 mol%. It was demonstrated that the type of MAO used as a cocatalyst affec
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Tanley, Simon W. M., Laurina-Victoria Starkey, Lucinda Lamplough, Surasek Kaenket, and John R. Helliwell. "The binding of platinum hexahalides (Cl, Br and I) to hen egg-white lysozyme and the chemical transformation of the PtI6octahedral complex to a PtI3moiety bound to His15." Acta Crystallographica Section F Structural Biology Communications 70, no. 9 (2014): 1132–34. http://dx.doi.org/10.1107/s2053230x14014009.

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This study examines the binding and chemical stability of the platinum hexahalides K2PtCl6, K2PtBr6and K2PtI6when soaked into pre-grown hen egg-white lysozyme (HEWL) crystals as the protein host. Direct comparison of the iodo complex with the chloro and bromo complexes shows that the iodo complex is partly chemically transformed to a square-planar PtI3complex bound to the Nδatom of His15, a chemical behaviour that is not exhibited by the chloro or bromo complexes. Each complex does, however, bind to HEWL in its octahedral form either at one site (PtI6) or at two sites (PtBr6and PtCl6). As heav
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Sengupta, Gargi, Pragati Pandey, Subhabrata De, Ramesh Ramapanicker, and Jitendra K. Bera. "A bromo-capped diruthenium(i,i) N-heterocyclic carbene compound for in situ bromine generation with NBS: catalytic olefin aziridination reactions." Dalton Transactions 47, no. 34 (2018): 11917–24. http://dx.doi.org/10.1039/c8dt01851k.

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Farag, Abeer Mohamed, Teoh Siang Guan, Hasnah Osman, Madhukar Hemamalini та Hoong-Kun Fun. "catena-Poly[[[aquamanganese(III)]-μ-(E)-5-bromo-N-[2-(5-bromo-2-oxidobenzylideneamino)-4-nitrophenyl]-2-oxidobenzamidato]N,N-dimethylfomamide monosolvate]". Acta Crystallographica Section E Structure Reports Online 68, № 4 (2012): m365—m366. http://dx.doi.org/10.1107/s1600536812008501.

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The asymmetric unit of the title complex, {[Mn(C20H10Br2N3O5)(H2O)]·(CH3)2NCHO}n, consists of one MnIIIion, one (E)-5-bromo-N-[2-(5-bromo-2-oxidobenzylideneamino)-4-nitrophenyl]-2-oxidobenzamidate ligand (Schiff base), one water molecule and anN,N-dimethylformamide molecule. The coordination geometry around the MnIIIion is a distorted octahedron, being surrounded by two O and two N atoms from the Schiff base, which are positioned in the equatorial plane. The water molecule and the O atom of the carbonyl group from the adjacent MnIIIcomplex are situated at the axial positions, leading to a poly
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Kyri, A. W., G. Schnakenburg, and R. Streubel. "A novel route to C-unsubstituted 1,2-oxaphosphetane and 1,2-oxaphospholane complexes." Chemical Communications 52, no. 55 (2016): 8593–95. http://dx.doi.org/10.1039/c6cc04667c.

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The synthesis of 1,2-oxaphosphetane complexes 7 and 1,2-oxaphospholane complex 12 bearing only substituents at phosphorus is reported using the reaction of Li/Cl phosphinidenoid complex 2 with 2-iodoethanol or 3-bromo-propane-1-ol and the subsequent dehydrohalogenation using KHMDS.
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Zhao, Yun, Xiao-Feng Shen, and Li-Fang Zhang. "A new mononuclear neutral high-spin iron(III) complex with the different tridentate ligands 5-bromosalicylaldehyde (pyridin-2-yl)hydrazone and 5-bromosalicylaldehyde thiosemicarbazone." Acta Crystallographica Section E Crystallographic Communications 74, no. 2 (2018): 252–55. http://dx.doi.org/10.1107/s2056989018001263.

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The title neutral mononuclear complex, [1-(5-bromo-2-oxidobenzylidene)thiosemicarbazidato](4-bromo-2-{[2-(pyridin-2-yl)hydrazinylidene]methyl}phenolato)iron(III), [Fe(C8H6BrN3OS)(C12H9BrN3O)] (I), crystallizes in the monoclinic space group C 2/c and has two different planar tridentate ligands. The central FeIII ion is coordinated to three N, two O and one S atom, forming a distorted octahedral FeN3O2S coordination geometry. In the crystal, the complex molecules are linked by N—H...O and N—H...N hydrogen bonds and π–π interactions into layers parallel to (100). Magnetic measurements show that t
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Dissertations / Theses on the topic "Bromo complex"

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Khan, Mustayeen Ahmed. "Stabilite, spectres electroniques et structures des halogenocuprates en milieu protique." Université Louis Pasteur (Strasbourg) (1971-2008), 1988. http://www.theses.fr/1988STR13059.

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Etude des complexes de cu(ii) dans les solvants protiques l'eau, le methanol et l'acide acetique. On caracterise 4 complexes successsifs; calcul de leurs constantes de stabilite. Etude de l'effet du solvant sur les spectres electroniques
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Bouet, Gilles. "Etude structurale et analytique de complexes d'halogénures d'éléments 3D : mx::(2) (M = co,ni,cu; X = cl,br) et de diverses aldoximes furanniques." Angers, 1987. http://www.theses.fr/1987ANGE0009.

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Vingt-quatre nouveaux complexes d'halogénures de métaux 3 D : mx::(2) (m = co,ni,cu; x = cl,br) sont préparés et caractérisés. Leurs structures sont déterminées par diffraction des rayons X pour deux des composés et, à partir de celles-ci, pour l'ensemble des complexes grâce à la spectroscopie infrarouge et à la spectroscopie électronique. Le calcul des constantes de stabilité et des paramètres thermodynamiques correspondants par titrimétrie thermométrique est décrit.
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Foulet-Fonseca, Gloria. "Etude par spectroscopie vibrationnelle des complexes méthylcarbyniques et méthylcarbéniques de chrome." Paris 13, 1987. http://www.theses.fr/1987PA132028.

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Etude en particulier de complexes, du type br(co)::(4)crcch::(3), br(co)::(4)crcchd::(2) et d'une série de mélanges isotopiques. Mise en évidence de la non-équivalence des liaisons c-h du groupe methyle. Etablissement d'un champ de forces pour les complexes méthylcarbyniques
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Laurent, Pascale. "Complexes acyl, alcoxycarbonyl et alkyl tetracarbonylfer : intermédiaires dans la carbonylation catalytique d'halogénures d'alkyle." Brest, 1989. http://www.theses.fr/1989BRES2002.

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MULYADI, EDDY. "Le complexe de bromo-tengger (est java, indonesie). Etude structurale et volcanologique." Clermont-Ferrand 2, 1992. http://www.theses.fr/1992CLF21453.

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Le massif de bromo-tengger est un volcan composite. Cet ensemble resulte de la juxtaposition de plusieurs appareils d'importances inegales: l'appareil de nongkojajar (age <1,4 ma), le plus ancien, est constitue essentiellement de coulees. Il a probablement ete affecte par un glissement de flanc, puis un effondrement calderique de type krakatau. L'appareil de ngadisari (age <82000 ans) est fait d'une succession d'epaisses coulees. Il a ete affecte par trois phases de destruction (calderas de type krakatau). L'appareil de tengger sensu stricto (age <265000 ans) est aussi constitue de coulees. Il
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Dohi, Koji. "Studies on the RNA-dependent RNA polymerase complex of brome mosaic virus." Kyoto University, 2005. http://hdl.handle.net/2433/144993.

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Kyoto University (京都大学)<br>0048<br>新制・論文博士<br>博士(農学)<br>乙第11674号<br>論農博第2557号<br>新制||農||912(附属図書館)<br>学位論文||H17||N4057(農学部図書室)<br>23487<br>UT51-2005-D592<br>京都大学大学院農学研究科農林生物学専攻<br>(主査)教授 奥野 哲郎, 教授 遠藤 隆, 教授 西岡 孝明<br>学位規則第4条第2項該当
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Avila, Julia Maria Machado de. "Estudo da complexação da 5-amino-6-bromo-8-hidroxi-1,4-naftoquinona com metais de transição." reponame:Biblioteca Digital de Teses e Dissertações da UFRGS, 1998. http://hdl.handle.net/10183/24066.

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Os derivados substituídos das 1,4-naftoquinonas podem coordenar-se a metais e assim, apresentar aplicações em diferentes áreas, como por exemplo, em biologia e química analítica. Neste trabalho foi estudada a coordenação da 5-amino- 6-bromo-8-hidróxi-1 ,4-nattoquinona aos íons metálicos divalentes Ni", Cu", Co", VO" e Pd" e averiguado seu potencial antibacteriano. As reações realizadas basearam-se em diferentes métodos de síntese, de forma a se obter o melhor rendimento. Os compostos obtidos foram caracterizados por espectroscopia na região do infravermelho (IV) e do ultravioleta-visível (UVVI
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Monteil, Fanny. "Carbonylation de l'oct-1-ène et du bromobenzène catalysée par des complexes hydrosolubles du palladium ou du rhodium." Toulouse, INPT, 1993. http://www.theses.fr/1993INPT044G.

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Dans le but d'assurer un recyclage aise du complexe organometallique dans un procede utilisant la catalyse homogene, les derives rh#2(s#tbu)#2(co)#2l#2, (1) et pdl#3, (2) ont ete synthetises avec un ligand l hydrosoluble, la tris(m-sulfonatophenyl)phosphine. Dans la reaction d'hydroformylation de l'oct-1-ene, un cosolvant est ajoute pour ameliorer le transfert du substrat dans la phase aqueuse contenant le complexe (1) tout en minimisant les quantites d'eau dans la phase organique. La vitesse de reaction est augmentee, mais le complexe evolue vers l'espece hrh(co)l#3 qui, au detriment de l'act
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Mercier-Girardot, Sophie. "Réactions d'élimination-addition sur le 5-bromo-3,4-dihydro-2h-pyrane réalisées au moyen des bases complexes : synthèse de composés tricycliques cyclopentaniques mono ou bisoxygènes." Nancy 1, 1995. http://www.theses.fr/1995NAN10060.

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L’action des bases complexes sur le 5-bromo-3,4-dihydropyrane a permis d'engendrer pour la première fois des intermédiaires a courte durée de vie de type déhydrodihydropyrane et de leur condenser des nucléophiles tels que les énolates de cétones. La nature des produits obtenus qui dépend du type d'énolate condense nous a conduit à proposer un mécanisme pour ces réactions d'élimination-addition. D’un point de vue synthétique, ces réactions ont abouti à la formation d'alcools méthylènes cyclobutaniques hétérocycliques et de composes cétoniques possédant le motif déhydropyrane sur la molécule, av
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Galão, Rui Pedro Ribeiro. "Role of the cellular decapping activator LSM1-7 complex in the replication of positive-strand RNA viruses." Doctoral thesis, Universitat Pompeu Fabra, 2010. http://hdl.handle.net/10803/7222.

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By using the ability of the positive-strand RNA ((+)RNA) virus BMV to replicate in yeast it was previously shown that subunits of the LSm1-7 ring, as well as Pat1 and Dhh1 play an essential role in the transit of the BMV genome from translation to replication. In non-infected cells, these proteins mediate the transition of cellular mRNAs from a translational to a non-translational state by activating decapping in the 5'-3' - deadenylation-dependent mRNA decay pathway. Given the conservation of this pathway from yeast to humans and the common need of all (+)RNA viruses to regulate the transitio
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Books on the topic "Bromo complex"

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Walters, Dale. Chocolate Crisis. University Press of Florida, 2021. http://dx.doi.org/10.5744/florida/9781683401674.001.0001.

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Chocolate is the center of a massive global industry worth billions of dollars annually, yet its future in our modern world is currently under threat. Here, Dale Walters discusses the problems posed by plant diseases, pests, and climate change, looking at what these mean for the survival of the cacao tree. Walters takes readers to the origins of the cacao tree in the Amazon basin of South America, describing how ancient cultures used the beans produced by the plant, and follows the rise of chocolate as an international commodity over many centuries. He explains that most cacao is now grown on
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Book chapters on the topic "Bromo complex"

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of hydrazine bridged chromium(II) bromo complex." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54228-6_173.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of iron(II) bromo complex with aminodiphosphine." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54231-6_117.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of manganese(II) complex with 4-bromo-3,5-dimethylpyrazole and 4-bromo-3,5-dimethylpyrazolate." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54228-6_348.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of copper(II) bromo complex with neutral malonamide." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-53974-3_539.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of iron(II) bromo complex with polythioether ligand." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54231-6_68.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of nickel(II) bromo complex with 2-aminoethanol." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54234-7_290.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of iron(III) bromo complex with oxydiacetic acid." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54231-6_165.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of nickel(II) bromo complex with neutral malonamide." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-53971-2_780.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of manganese(II) bromo complex with neutral malonamide." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-49202-4_753.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of copper(II) bromo complex with formylpyrazineN(4)-methylthiosemicarbazone." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54237-8_57.

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Conference papers on the topic "Bromo complex"

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Herder, Just L., and Arend L. Schwab. "On Dynamically Equivalent Force Systems and Their Application to the Balancing of a Broom or the Stability of a Shoe Box." In ASME 2004 International Design Engineering Technical Conferences and Computers and Information in Engineering Conference. ASMEDC, 2004. http://dx.doi.org/10.1115/detc2004-57188.

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The stability of a rigid body on which two forces are in equilibrium can be assessed intuitively. In more complex cases this is no longer true. This paper presents a general method to assess the stability of complex force systems, based on the notion of dynamic equivalence. A resultant force is considered dynamically equivalent to a given system of forces acting on a rigid body if the contributions to the stability of the body of both force systems are equal. It is shown that the dynamically equivalent resultant force of two given constant forces applies at the intersection of its line of acti
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