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Journal articles on the topic "TCNZ"
Wolfram, Benedikt, Çağla Baş, Christian Kleeberg, and Martin Bröring. "Interaction of manganese corroles with TCNQ and related acceptor molecules." Journal of Porphyrins and Phthalocyanines 24, no. 05n07 (May 2020): 705–11. http://dx.doi.org/10.1142/s1088424619501359.
Full textMaity, Amarendra N., Brigitte Schwederski, Biprajit Sarkar, Stanislav Záliš, Jan Fiedler, Sanjib Kar, Goutam K. Lahiri, et al. "Tetranuclear Complexes of [Fe(CO)2(C5H5)]+with TCNX Ligands (TCNX = TCNE, TCNQ, TCNB): Intramolecular Electron Transfer Alternatives in Compounds (μ4-TCNX)[MLn]4." Inorganic Chemistry 46, no. 18 (September 2007): 7312–20. http://dx.doi.org/10.1021/ic062253k.
Full textWaldhör, Eberhard, Wolfgang Kaim, Max Lawson, and Jeanne Jordanov. "Paramagnetism of Tetranuclear Complexes between TCNX Ligands (TCNE, TCNQ, TCNB) and Four Pentaammineruthenium or Dicarbonyl(pentamethylcyclopentadienyl)manganese Fragments." Inorganic Chemistry 36, no. 15 (July 1997): 3248–52. http://dx.doi.org/10.1021/ic960998s.
Full textGurney, Jason K., James Stanley, Katherine McGlynn, Lorenzo Richiardi, Caroline Shaw, Richard Edwards, Tony R. Merriman, et al. "Testicular Cancer in New Zealand (TCNZ) study: protocol for a national case–control study." BMJ Open 8, no. 8 (August 2018): e025212. http://dx.doi.org/10.1136/bmjopen-2018-025212.
Full textBerger, Sascha, Heiko Hartmann, Matthias Wanner, Jan Fiedler, and Wolfgang Kaim. "Tetranuclear complexes {(μ4-TCNX)[Cu(Me3TACN)]4}(BF4)4 with TCNX=TCNE, TCNQ or TCNB (1,2,4,5-tetracyanobenzene) and Me3TACN=1,4,7-trimethyl-1,4,7-triazacyclononane." Inorganica Chimica Acta 314, no. 1-2 (March 2001): 22–26. http://dx.doi.org/10.1016/s0020-1693(00)00368-6.
Full textXu Hong-Bin and Wang Yuan-Xu. "First-principles study of low-compressibility of transition-metal Tc and its nitrides TcN,TcN2,TcN3 and TcN4." Acta Physica Sinica 58, no. 8 (2009): 5645. http://dx.doi.org/10.7498/aps.58.5645.
Full textHartmann, Heiko, Wolfgang Kaim, Matthias Wanner, Axel Klein, Stéphanie Frantz, Carole Duboc-Toia, Jan Fiedler, and Stanislav Záliš. "Proof of Innocence for the Quintessential Noninnocent Ligand TCNQ in Its Tetranuclear Complex with Four [fac-Re(CO)3(bpy)]+Groups: Unusually Different Reactivity of the TCNX Ligands (TCNX = TCNE, TCNQ, TCNB)‖." Inorganic Chemistry 42, no. 22 (November 2003): 7018–25. http://dx.doi.org/10.1021/ic034232l.
Full textKrishna, Marothu Vamsi, and Dannana Gowri Sankar. "Utility of σ and π-Acceptors for the Spectrophotometric Determination of Gemifloxacin Mesylate in Pharmaceutical Formulations." E-Journal of Chemistry 5, no. 3 (2008): 493–98. http://dx.doi.org/10.1155/2008/801545.
Full textSrinivasa Rao, Pedada, Avinash L. Puyad, Sidhanath V. Bhosale, and Sheshanath V. Bhosale. "Triphenylamine-Merocyanine-Based D1-A1-π-A2/A3-D2 Chromophore System: Synthesis, Optoelectronic, and Theoretical Studies." International Journal of Molecular Sciences 20, no. 7 (April 1, 2019): 1621. http://dx.doi.org/10.3390/ijms20071621.
Full textYun, Sungryul, Seongcheol Mun, Seung Koo Park, Inwook Hwang, and Meejeong Choi. "A Thermo–Mechanically Robust Compliant Electrode Based on Surface Modification of Twisted and Coiled Nylon–6 Fiber for Artificial Muscle with Highly Durable Contractile Stroke." Polymers 14, no. 17 (August 31, 2022): 3601. http://dx.doi.org/10.3390/polym14173601.
Full textDissertations / Theses on the topic "TCNZ"
Ross, Peter, and n/a. "Organisational and Workforce Restructuring in a Deregulated Environment: A Comparative Study of The Telecom Corporation of New Zealand (TCNZ) and Telstra." Griffith University. Graduate School of Management, 2003. http://www4.gu.edu.au:8080/adt-root/public/adt-QGU20030930.155125.
Full textRoss, Peter. "Organisational and Workforce Restructuring in a Deregulated Environment: A Comparative Study of The Telecom Corporation of New Zealand (TCNZ) and Telstra." Thesis, Griffith University, 2003. http://hdl.handle.net/10072/367438.
Full textThesis (PhD Doctorate)
Doctor of Philosophy (PhD)
Graduate School of Management
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Silva, Maria do Socorro de Paula. "SÃntese e caracterizaÃÃo de complexos bipiridÃnicos de rutÃnio com ligantes polinitrilados." Universidade Federal do CearÃ, 2007. http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=1453.
Full textNo presente trabalho, os complexos cis-[Ru(dcbpy)(bpy)(TCNQ)Cl] e cis-[Ru(dcbpy)(bpy)(TCNE)Cl], denominados de Ru-TCNQ e Ru-TCNE, respectivamente, (dcbpy = 4,4â-dicarboxi-2,2â-bipiridina e bpy = 2,2â-bipirina) foram sintetizados e caracterizados por tÃcnicas espectroscÃpicas e eletroquÃmicas. Os espectros de UV-VisÃvel apresentaram para os complexos Ru-TCNQ e Ru-TCNE bandas de absorÃÃo na regiÃo do visÃvel, sendo atribuÃdas Ãs bandas de transferÃncia de carga do tipo MLCT. Os espectros de luminescÃncia apresentaram emissÃo, quando excitados na regiÃo da MLCT (500nm), evidenciando a modificaÃÃo estrutural com a coordenaÃÃo dos ligantes polinitrilados ao RuII. Os decaimentos dos compostos forma biexponenciais, com o complexo Ru-TCNQ apresentou tempos de vida muito mais curtos que o Ru-TCNE. No infravermelho, foi observado que os compostos TCNX encontram-se ligados covalentemente ao Ãtomo de rutÃnio. Essa coordenaÃÃo se dà atravÃs de ligaÃÃo σ entre o Ãtomo de nitrogÃnio de uma das nitrilas, evidenciada pelo surgimento de um maior nÃmero de bandas referentes ao estiramento C≡N, comparativamente aos ligantes livres de coordenaÃÃo. A observaÃÃo do deslocamento dessas bandas para regiÃes de menor energia, quando comparadas aos ligantes livres, permitiram identificar que os ligantes TCNQ e TCNE encontram-se coordenados em sua forma radicalar (TCNX.â). O grau de transferÃncia de carga (Z) baseado nos espectros de infravermelho para os compostos Ru-TCNQ e Ru-TCNE foi de 0,66 e 0,78, respectivamente. Os espectros de RPE confirmaram a coordenaÃÃo dos ligantes ao centro metÃlico na forma reduzida (Ru-TCNQ: g = 2,007 e para Ru-TCNE: g = 2,010). Os potencias redox nos complexos Ru-TCNQ (Ered = 0,70V vs ENH) e Ru-TCNE (Ered = 1,30V vs ENH) foram deslocados para potenciais mais positivos, quando comparados ao precursor cis-[Ru(dcbpy)(bpy)Cl2] (Ered = 0,67V vs ENH), evidenciando o forte carÃter π receptor de elÃtrons dos ligantes TCNX, estabilizando o centro metÃlico na forma reduzida. Esses resultados evidenciam um carÃter retirador de elÃtrons mais pronunciado para o ligante TCNE em relaÃÃo ao TCNQ.
In this work, the [Ru(bpy)(dcbpy)(TCNQ)Cl] and [Ru(bpy)(dcbpy)(TCNE)Cl] complexes, called Ru-TCNQ and Ru-TCNE, respectively, where bpy = 2,2â- bipyridine and dcbpy = 4,4â-dicarboxy-2,2â-bipyridine, were synthesized and characterized by spectroscopy and electrochemical techniques. The absorption spectra of the Ru-TCNQ and Ru-TCNE complexes showed bands assigned to metalto-ligand charge transfer transitions (MLCT). The luminescence spectra, with excitation at the MLCT, exhibited emission with maximum of intensity at 570 and 605 nm for the Ru-TCNQ and Ru-TCNE complexes, respectively. The luminescence decay of the complexes follows a biexponential law, with the Ru-TCNQ complex showing shorter lifetime than the Ru-TCNE complex. The infrared vibrational spectra of the complexes show a larger number of nitrile stretching bands, comparatively to the free ligands of coordination. These suggesting that the TCNX compounds are coordinated to the ruthenium atom. Upon coordenation, the shifts of these bands for lower energy values are indicative of the TCNX reduced form (TCNX⋅â). These results are confirmed by EPR spectra with g = 2.007 and 2.010 for Ru-TCNQ and Ru-TCNE complexes, respectively. The degree of charge transfer (Z) for the Ru-TCNQ and Ru-TCNE compounds was evaluated as 0.66 and 0.78, respectively. The RuIII/II redox potentials of the Ru-TCNQ (0.70V) and Ru-TCNE (1.30V) compounds, shifted for more positive potentials, when compared to the starting complex, cis- [Ru(dcbpy)(bpy)Cl2] (0,67V). These results inducate that the ligands acts as π-acceptor allowing a π-back-bonding interaction which imply in a thermodynamic stability of the metal in the reduced state (RuII). The data, all together, suggest that the TCNE compound presents a higher πback-bonding interaction capability than TCNQ compound.
Pontes, Daniel de Lima. "Estudo de complexos de ferro-cyclam com ligantes carboxilados e polinitrilados." Universidade Federal do CearÃ, 2006. http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=2934.
Full textO objetivo deste trabalho à contribuir com o desenvolvimento da quÃmica do sistema Fe-cyclam, atravÃs da sÃntese e caracterizaÃÃo de novos complexos metÃlicos deste sistema com duas classes de ligantes: carboxilados (oxalato e acetato) e ligantes polinitrilados (7,7,8,8 âtetracianoquinodimetano e tetracianoetileno ). AtravÃs da caracterizaÃÃo do complexo cis-[Fe(cyclam)ox]PF6 por infravermelho foi possÃvel identificar que o ligante oxalato encontra-se coordenado ao centro metÃlico de forma bidentada, bem como garantir que o ligante macrocÃclico cyclam continua na esfera de coordenaÃÃo do metal. O potencial formal de meia onda do processo redox Fe3+/2+ do complexo foi observado em â39mV vs Ag/AgCl. O potencial observado encontra-se deslocado 240mV para menores valores em relaÃÃo ao complexo precursor, favorecendo ao estado de oxidaÃÃo Fe3+ do metal, devido ao maior efeito σ doador do ligante oxalato frente aos cloretos. O espectro UV-Vis do complexo cisâ[Fe(cyclam)ox]PF6, em meio aquoso, apresentou trÃs bandas: 229nm, atribuÃda a uma transiÃÃo intraligante do cyclam, 293nm e 357nm, atribuÃdas à transferÃncia de carga de orbitais π do ligante para o orbitais dπ* do metal. Os experimentos fotoquÃmicos demonstraram a grande sensibilidade do complexo à luz, sendo observado a labilizaÃÃo do ligante oxalato da esfera de coordenaÃÃo do metal, e a reatividade da espÃcie formada atravÃs da obtenÃÃo do complexo trans-[Fe(cyclam)acet2]PF6, AtravÃs do estudo de Raio-X, obtido a partir do cristal do complexo trans-[Fe(cyclam)acet2]PF6, foi possÃvel comprovar o modo de coordenaÃÃo das duas molÃculas de acetato na posiÃÃo trans, bem como a identificaÃÃo da disposiÃÃo do cyclam no plano da molÃcula atravÃs de um arranjo conformacional trans-III. Os espectros no infravermelho dos complexos cis - [Fe(cyclam)(TCNX)Cl]Cl, onde TCNX representa os ligantes TCNQ ou TCNE, apresentaram um maior nÃmero de bandas referentes aos estiramentos CN, comparativamente aos ligantes livres, confirmando a alteraÃÃo da simetria do ligante causada pela coordenaÃÃo do metal. Com base nos deslocamentos destas freqÃÃncias para menores valores, comparativamente ao ligante livre, foi possÃvel identificar que os ligantes TCNQ e TCNE estÃo coordenados em sua forma radicalar, estado de oxidaÃÃo â1, sugerindo assim a ocorrÃncia de um processo de transferÃncia de elÃtrons do centro metÃlico, previamente reduzido (Fe2+), para os ligantes TCNX. Os potenciais redox dos Ãtomos de ferro, nos complexos com os ligantes polinitrialados TCNQ (693mV vs ENH) e TCNE (854mV vs ENH), foram deslocados para potenciais mais positivos, comparativamente ao observado no complexo precursor cis-[Fe(cyclam)Cl2]Cl (405mV vs ENH), indicando assim um forte deslocamento de densidade eletrÃnica dπ para os orbitais de simetria π dos ligantes TCNX. Os processos centrados nos ligantes coordenados ficaram mais prÃximos do que nos ligantes livres, indicando uma diminuiÃÃo na barreira de transferÃncia de elÃtrons, que segundos dados da literatura leva a uma melhor conduÃÃo elÃtrica. Os espectros eletrÃnicos dos complexos, em meio aquoso, apresentaram uma banda localizada em baixa energia, atribuÃda a transferÃncias de carga do tipo LMCT dos orbitais pπ das molÃculas de TCNX, para os orbitais dπ* do Ãon Fe3+. No complexo com o ligante TCNQ, esta banda aparece em 764nm e no complexo com o ligante TCNE, em 861nm. Observa-se ainda nos dois complexos a presenÃa das bandas referentes Ãs transiÃÃes LMCT dos cloretos para o Ãon Fe3+ em regiÃes muito prÃximas, em 557 no complexo com TCNE e em 568nm no complexo com TCNQ. A presenÃa desta banda novamente sugere a presenÃa do Ferro no estado oxidado (Fe+3).
The main objective of this work is to contribute with the chemistry of the system Fe-Cyclam through the synthesis and characterization of complexes with carboxylate ligants, acetate and oxalate, and polinitrilate ligands, 7,7,8,8-tetracyanoquinodimethane (TCNQ) and tetracyanoethylene (TCNE). The infrared spectra of the cis-[Fe(cyclam)ox]PF6 complex allowed to identify the coordination of the oxalate ligand to the iron metal in a bidentate mode as well as to suggest the presence of the macrocycle in the coordination sphere of the metal. The redox potential of the complex was observed at â39mV vs Ag/AgCl. The potential is dislocated 240mV for more positive potential when compared to that observed for the precursor complex cis-[Fe(cyclamCl2]Cl. This effect can be attributed to the stronger σ effect of the oxalate ligand when compared to the chlorine. The UV-Vis spectra of the complex, presented three bands: 229nm, attributed to a cyclam intraligand transition and the bands 293nm and 357nm, referring to ligand to metal electronic transfer from π orbitals of the oxalate to dπ* of the metal. The photochemical experiments proved the great sensibility of the complex to the light presence, being observed the reactivity effect of the complex formed after the light exposition by the formation of the trans-[Fe(cyclam)acet2]PF6 complex. Through the Ray-X obtained of the crystal of the trans-[Fe(cyclam)acet2]PF6 complex was possible to identify the coordination of two molecules of acetate at the trans position, as well as to identify the disposition of the cyclam ligand on the plane in a trans-III arrange. The infrared spectrum of the complexes cis - [Fe(cyclam)(TCNX)Cl]Cl, where the TCNX represent the ligands TCNQ and TCNE, present a great number of bands referring to the νCN, when compared with the ligands not coordinated, confirming the symetry changed induced by the metal coordination. Through the wavenumber variation of these bands was possible to identify that the TCNQ and TCNE ligands are coordinated in your radical way, oxidation state â1, suggestion this way the occurrence of a electron transfer from the iron, previously reduced (Fe+2), to the TCNX ligands. The redox potentials of the iron metals in the complexes with the polinitrilate ligands TCNQ (693mV vs ENH) and TCNE (854mV vs ENH) were dislocated for more positive potentials, when compared to the cis-[Fe(cyclam)Cl2]Cl precursor complex (405mV vs ENH), indicating the occurrence of an electronic density transfer to the TCNX molecules. The two potentials of the ligands on the complexes were closer than the ligands not coordinated, this approximation of the potential indicate a decrease of the inner electron transfer. The electronic spectra of the complexes, showed bands in the low energy region, attributed to a charge transfer LMCT, from the TCNX pπ orbital to the metal dπ* orbital. In the cis-[Fe(cyclam)(TCNQ)Cl]Cl complex, the band was observed at 764nm while in the complex with the TCNE ligand this band was observed at 861nm. Also, the complexes presented bands at 557nm (TCNE complex) and 568nm (TCNQ complex)referring to the LMCT transitions from the chlorine atoms to the iron metal reinforcing the assignment of the (Fe+3) oxidation state for the metal center.
Silva, Maria. "Síntese e caracterização de complexos bipiridínicos de rutênio com ligantes polinitrilados." reponame:Repositório Institucional da UFC, 2007. http://www.repositorio.ufc.br/handle/riufc/2079.
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In this work, the [Ru(bpy)(dcbpy)(TCNQ)Cl] and [Ru(bpy)(dcbpy)(TCNE)Cl] complexes, called Ru-TCNQ and Ru-TCNE, respectively, where bpy = 2,2’- bipyridine and dcbpy = 4,4’-dicarboxy-2,2’-bipyridine, were synthesized and characterized by spectroscopy and electrochemical techniques. The absorption spectra of the Ru-TCNQ and Ru-TCNE complexes showed bands assigned to metalto-ligand charge transfer transitions (MLCT). The luminescence spectra, with excitation at the MLCT, exhibited emission with maximum of intensity at 570 and 605 nm for the Ru-TCNQ and Ru-TCNE complexes, respectively. The luminescence decay of the complexes follows a biexponential law, with the Ru-TCNQ complex showing shorter lifetime than the Ru-TCNE complex. The infrared vibrational spectra of the complexes show a larger number of nitrile stretching bands, comparatively to the free ligands of coordination. These suggesting that the TCNX compounds are coordinated to the ruthenium atom. Upon coordenation, the shifts of these bands for lower energy values are indicative of the TCNX reduced form (TCNX⋅–). These results are confirmed by EPR spectra with g = 2.007 and 2.010 for Ru-TCNQ and Ru-TCNE complexes, respectively. The degree of charge transfer (Z) for the Ru-TCNQ and Ru-TCNE compounds was evaluated as 0.66 and 0.78, respectively. The RuIII/II redox potentials of the Ru-TCNQ (0.70V) and Ru-TCNE (1.30V) compounds, shifted for more positive potentials, when compared to the starting complex, cis- [Ru(dcbpy)(bpy)Cl2] (0,67V). These results inducate that the ligands acts as π-acceptor allowing a π-back-bonding interaction which imply in a thermodynamic stability of the metal in the reduced state (RuII). The data, all together, suggest that the TCNE compound presents a higher πback-bonding interaction capability than TCNQ compound.
No presente trabalho, os complexos cis-[Ru(dcbpy)(bpy)(TCNQ)Cl] e cis-[Ru(dcbpy)(bpy)(TCNE)Cl], denominados de Ru-TCNQ e Ru-TCNE, respectivamente, (dcbpy = 4,4’-dicarboxi-2,2’-bipiridina e bpy = 2,2’-bipirina) foram sintetizados e caracterizados por técnicas espectroscópicas e eletroquímicas. Os espectros de UV-Visível apresentaram para os complexos Ru-TCNQ e Ru-TCNE bandas de absorção na região do visível, sendo atribuídas às bandas de transferência de carga do tipo MLCT. Os espectros de luminescência apresentaram emissão, quando excitados na região da MLCT (500nm), evidenciando a modificação estrutural com a coordenação dos ligantes polinitrilados ao RuII. Os decaimentos dos compostos forma biexponenciais, com o complexo Ru-TCNQ apresentou tempos de vida muito mais curtos que o Ru-TCNE. No infravermelho, foi observado que os compostos TCNX encontram-se ligados covalentemente ao átomo de rutênio. Essa coordenação se dá através de ligação σ entre o átomo de nitrogênio de uma das nitrilas, evidenciada pelo surgimento de um maior número de bandas referentes ao estiramento C≡N, comparativamente aos ligantes livres de coordenação. A observação do deslocamento dessas bandas para regiões de menor energia, quando comparadas aos ligantes livres, permitiram identificar que os ligantes TCNQ e TCNE encontram-se coordenados em sua forma radicalar (TCNX.–). O grau de transferência de carga (Z) baseado nos espectros de infravermelho para os compostos Ru-TCNQ e Ru-TCNE foi de 0,66 e 0,78, respectivamente. Os espectros de RPE confirmaram a coordenação dos ligantes ao centro metálico na forma reduzida (Ru-TCNQ: g = 2,007 e para Ru-TCNE: g = 2,010). Os potencias redox nos complexos Ru-TCNQ (Ered = 0,70V vs ENH) e Ru-TCNE (Ered = 1,30V vs ENH) foram deslocados para potenciais mais positivos, quando comparados ao precursor cis-[Ru(dcbpy)(bpy)Cl2] (Ered = 0,67V vs ENH), evidenciando o forte caráter π receptor de elétrons dos ligantes TCNX, estabilizando o centro metálico na forma reduzida. Esses resultados evidenciam um caráter retirador de elétrons mais pronunciado para o ligante TCNE em relação ao TCNQ.
Monezi, Natália Mariana. "Espectroscopia Raman ressonante e cálculos DFT de sistemas modelo de transferência de carga." Universidade de São Paulo, 2018. http://www.teses.usp.br/teses/disponiveis/46/46136/tde-24082018-095811/.
Full textIn this work the charge transfer complexes resulting from the interaction between tetracyanoethylene (TCNE) and 7,7,8,8-tetracyanoquinodimethane (TCNQ), as electron accepting species and mono, bi and tri aromatic amines, as electron donating species, were studied in solution. Also the electrophilic aromatic substitution that occurs between the TCNE and amines has been studied. For this study, the spectroscopic techniques of UV-VIS absorption and Raman were used, which allowed the characterization of the charge transfer complexes, as well as of the species involved in the reaction of tricianovinylation that occurs between amines and TCNE. In order to support the experimental data, DFT (Density Functional Theory) and TDDFT (Time-dependent Density Functional Theory) calculations were performed, to obtain the optimized geometries, Raman frequency values and theoretical transition energies of such species. The electronic spectra of the complexes formed between TCNE and monoaromatic amines showed that their transition energies are proportional to the amine electron donation capacity. In fact it could be linearly correlated with the ionization potential values of the amines, following the Mullikens rule. The Raman spectra allowed to verify that the vibrational modes of the TCNE involved in the process of charge transfer, were displaced to lower wavenumbers with the reduction of the ionization potential of the amine, and analogously, a linear correlation between these two parameters could be obtained. In the case of bi and tri aromatic amines, the linear trend between transition energy and ionization potential was observed, but not for the Raman shifts of the TCNE bands. In the reaction of tricianovinylation, the electronic spectra enabled the identification of the participating species in the reaction, and their vibrational characterization by resonance Raman. Using resonance Raman spectroscopy, it was possible to characterize the intermediate species of the tricianovinylation reaction between TCNE and aromatic amines for the first time. The complexes involving TCNQ and monoaromatic amines showed a similar trend to that observed in complexes with TCNE. The transition energies of these complexes decrease linearly, as well as the vibrational modes of the TCNQ, which present shifts to lower Raman frequencies with the decrease of the ionization potential of the amine. On the other hand, complexes formed by TCNQ and amines with more than one aromatic ring in their structure do not present correlation between donor ionization potential and transition energy and Raman displacements. The calculations of the electronic and vibrational spectra presented good agreement with those obtained experimentally, however some limitations were evidenced in the description of the π interactions in these model systems.
Decoster, Marc, and E. Guerchais-Jacques. "Contribution à l'étude de la réactivite de polynitriles neutres et anioniques : comportement de TCNQ et TCNE vis-a-vis de complexes du molybdène ; propriétés électrochimiques et complexantes d'anions polycyanocarbones." Brest, 1994. http://www.theses.fr/1994BRES2017.
Full textKirui, Joseph Kiprono. "ESR study of DMTM(TCNQ)₂." Thesis, University of British Columbia, 1990. http://hdl.handle.net/2429/29191.
Full textScience, Faculty of
Physics and Astronomy, Department of
Graduate
Qureshi, Saleem. "Magnetic properties of TCNQ complexes." Thesis, University of Nottingham, 1990. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.278000.
Full textBeales, T. P. "Magnetic susceptibilities of TCNQ complex salts." Thesis, University of Nottingham, 1987. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.376162.
Full textBooks on the topic "TCNZ"
Vietnam. Tỏ̂ng cục tiêu chuả̂n đo lường chá̂t lượng., ed. Danh mục TCVN và TCN, 1993. [Hà Nội]: Tỏ̂ng cục tiêu chuả̂n đo lường chá̂t lượng, 1993.
Find full text1948-, Adams Kenneth M., and Rourke Byron P. 1939-, eds. The TCN guide to professional practice in clinical neuropsychology. Amsterdam: Swets & Zeitlinger, 1992.
Find full textLaMondia, James Arthur. TCN tracker: A decision-based cyst nematode management aid for Connecticut wrapper tobacco types. New Haven: Connecticut Agricultural Experiment Station, 2003.
Find full textLaMondia, James Arthur. TCN tracker: A decision-based cyst nematode management aid for Connecticut wrapper tobacco types. New Haven: Connecticut Agricultural Experiment Station, 2003.
Find full textLobo, Cecilia Lanza. Mayo y después: La rebelión del Tcnl. Emilio Lanza contra García Meza : los últimos días de la dictadura. La Paz: [s.n.], 1995.
Find full textGraja, Andrzej. Les interactions électron-électron et électron-phonon dans les systèmes unidimensionnels des sels de TCNQ: Nature et conséquences spectrales. Varsovie: Editions scientifiques de Pologne, 1985.
Find full textAdams & Rourke. TCN Guide to Professional Practice I. Garland Science, 1992.
Find full textAdams & Rourke. Tcn Guide to Professional (Hcb) Practice. Garland Science, 1992.
Find full text2022 TCNA Handbook for Ceramic, Glass, and Stone Tile Installation. TCNA, 2022.
Find full textResnick, Robert, David Halliday, and Jearl Walker. Fundamentals of Physics Extended 10E All Access Pack with Gen Physics Lab 5E TCNJ Set. Wiley & Sons, Incorporated, John, 2014.
Find full textBook chapters on the topic "TCNZ"
Giliani, Silvia. "TCN2 Deficiency." In Encyclopedia of Medical Immunology, 632–34. New York, NY: Springer New York, 2020. http://dx.doi.org/10.1007/978-1-4614-8678-7_180.
Full textGiliani, Silvia. "TCN2 Deficiency." In Encyclopedia of Medical Immunology, 1–3. New York, NY: Springer New York, 2019. http://dx.doi.org/10.1007/978-1-4614-9209-2_180-1.
Full textCorvaja, C., L. Pasimeni, and A. Toffoletti. "Time Resolved EPR Studies of Phenazine-TCNQ and Biphenyl-TCNQ Excited Triplets." In 25th Congress Ampere on Magnetic Resonance and Related Phenomena, 24–25. Berlin, Heidelberg: Springer Berlin Heidelberg, 1990. http://dx.doi.org/10.1007/978-3-642-76072-3_10.
Full textBarišić, S., and A. Bjeliš. "Equilibrium Properties of TTF-TCNQ." In Theoretical Aspects of Band Structures and Electronic Properties of Pseudo-One-Dimensional Solids, 49–122. Dordrecht: Springer Netherlands, 1985. http://dx.doi.org/10.1007/978-94-009-5299-7_2.
Full textMahony, Brendan, and Jin Song Dong. "Sensors and actuators in TCOZ." In FM’99 — Formal Methods, 1166–85. Berlin, Heidelberg: Springer Berlin Heidelberg, 1999. http://dx.doi.org/10.1007/3-540-48118-4_12.
Full textMahony, Brendan, and Jin Song Dong. "Overview of the Semantics of TCOZ." In IFM’99, 66–85. London: Springer London, 1999. http://dx.doi.org/10.1007/978-1-4471-0851-1_5.
Full textDong, Jin Song, Ping Hao, Sheng Chao Qin, Jun Sun, and Wang Yi. "Timed Patterns: TCOZ to Timed Automata." In Formal Methods and Software Engineering, 483–98. Berlin, Heidelberg: Springer Berlin Heidelberg, 2004. http://dx.doi.org/10.1007/978-3-540-30482-1_39.
Full textMiller, Tim, and Peter McBurney. "Multi-agent System Specification Using TCOZ." In Multiagent System Technologies, 216–21. Berlin, Heidelberg: Springer Berlin Heidelberg, 2005. http://dx.doi.org/10.1007/11550648_20.
Full textKagoshima, Seiichi, Hiroshi Nagasawa, and Takashi Sambongi. "Properties of TTF-TCNQ and Its Family." In One-Dimensional Conductors, 48–105. Berlin, Heidelberg: Springer Berlin Heidelberg, 1988. http://dx.doi.org/10.1007/978-3-642-83179-9_3.
Full textGropas, Ruby. "Migrant Integration and the Role of the EU." In IMISCOE Research Series, 73–93. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-67284-3_4.
Full textConference papers on the topic "TCNZ"
Radulescu, Bogdan Alexandru, Adina Magda Florea, and Victorita Radulescu. "TCN Units, Solution in Recognition of Human Activities." In ASME 2021 30th Conference on Information Storage and Processing Systems. American Society of Mechanical Engineers, 2021. http://dx.doi.org/10.1115/isps2021-65039.
Full textYe Chunuan and Chen Guorong. "Photo emission spectroscopy for Ag-TCNQ (TCNQ = tetracyanoquinodimethane) nanowires." In 8th International Vacuum Electron Sources Conference and Nanocarbon (2010 IVESC). IEEE, 2010. http://dx.doi.org/10.1109/ivesc.2010.5644421.
Full textCortinas, R., J. M. Gonzaga, A. R. Green, A. M. Saulenas, and B. F. BuSha. "TCNJ Athlete Tracker." In 2015 41st Annual Northeast Biomedical Engineering Conference (NEBEC). IEEE, 2015. http://dx.doi.org/10.1109/nebec.2015.7117126.
Full textJanssen, P. "EPR in TEA(TCNQ)2 and MEM(TCNQ)2 at FIR frequencies." In 16th International Conference on Infrared and Millimeter Waves. SPIE, 1991. http://dx.doi.org/10.1117/12.2297833.
Full textZhou, Fei, Honghai Fan, Baoping Lu, Hongbao Zhang, Infant Raj, Xingang Tao, and Kankan Bai. "Application of DNN-TCN Composite Neural Network in Rate of Penetration Prediction." In IADC/SPE Asia Pacific Drilling Technology Conference and Exhibition. SPE, 2022. http://dx.doi.org/10.2118/209886-ms.
Full textQian, Feng, Chengyue Gong, Karishma Sharma, and Yan Liu. "Neural User Response Generator: Fake News Detection with Collective User Intelligence." In Twenty-Seventh International Joint Conference on Artificial Intelligence {IJCAI-18}. California: International Joint Conferences on Artificial Intelligence Organization, 2018. http://dx.doi.org/10.24963/ijcai.2018/533.
Full textWu, Hai, Qing Li, Chenglu Wen, Xin Li, Xiaoliang Fan, and Cheng Wang. "Tracklet Proposal Network for Multi-Object Tracking on Point Clouds." In Thirtieth International Joint Conference on Artificial Intelligence {IJCAI-21}. California: International Joint Conferences on Artificial Intelligence Organization, 2021. http://dx.doi.org/10.24963/ijcai.2021/161.
Full textJanssen, P. "FIR study of TeA(TcNq)2." In 15th International Conference on Infrared and Millimeter Waves. SPIE, 1990. http://dx.doi.org/10.1117/12.2301523.
Full textFernandez, David, Jaime Jimenez, Jon Andreu, Carlos Cuadrado, and Inigo Kortabarria. "A TCN Gateway Emulator." In 2007 IEEE International Symposium on Industrial Electronics. IEEE, 2007. http://dx.doi.org/10.1109/isie.2007.4375076.
Full textKelly, Terri-Ann N., Brendan L. Roach, Charles R. Mackenzie-Smith, Adam B. Nover, Eben G. Estell, Grace D. O’Connell, Gerard A. Ateshian, and Clark T. Hung. "Chondroitinase-ABC Digestion and Dynamic Loading Increase Tension-Compression Nonlinearity in Tissue-Engineered Cartilage." In ASME 2013 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2013. http://dx.doi.org/10.1115/sbc2013-14621.
Full textReports on the topic "TCNZ"
Li, Shulong, Henry S. White, and Michael D. Ward. Scanning Tunneling Microscopy of the Organic Semiconductor ((Eta-C5Me5) 2Ru(1,4-(2(2))-cyclophane)) (TCNQ)4. Fort Belvoir, VA: Defense Technical Information Center, February 1992. http://dx.doi.org/10.21236/ada246848.
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