Relevant bibliographies by topics / Cu(I)

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

Academic literature on the topic 'Cu(I)'

Author: Grafiati
Published: 4 June 2021
Last updated: 1 February 2022

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Journal articles on the topic "Cu(I)"

1

Ziegler, Micah S., K. V. Lakshmi, and T. Don Tilley. "Dicopper Cu(I)Cu(I) and Cu(I)Cu(II) Complexes in Copper-Catalyzed Azide–Alkyne Cycloaddition." Journal of the American Chemical Society 139, no. 15 (April 10, 2017): 5378–86. http://dx.doi.org/10.1021/jacs.6b13261.

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Sakurada, Takafumi, Hideki Maekawa, and Toshio Yokokawa. "Cu(II)/Cu(I)/Cu Redox in Alkali Borate Melts." Materials Transactions, JIM 39, no. 7 (1998): 740–46. http://dx.doi.org/10.2320/matertrans1989.39.740.

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Müller, Jürgen F. K., and Patrick Vogt. "Cu(I)-catalyzed sulfoximination." Tetrahedron Letters 39, no. 27 (July 1998): 4805–6. http://dx.doi.org/10.1016/s0040-4039(98)00925-3.

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4

Zhang, Xin, Jian-Kai Cheng, Ming-Jian Zhang, and Yuan-Gen Yao. "A new luminescent Cu(I) complex stabilized by Cu⋅⋅⋅Cu interactions." Inorganic Chemistry Communications 20 (June 2012): 101–4. http://dx.doi.org/10.1016/j.inoche.2012.02.027.

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Mezhenny, S., I. Lyubinetsky, W. J. Choyke, and J. T. Yates. "Electron stimulated decomposition of adsorbed hexafluoroacetylacetonate Cu(I) vinyltrimethylsilane, Cu(I)(hfac)(vtms)." Journal of Applied Physics 85, no. 6 (March 15, 1999): 3368–73. http://dx.doi.org/10.1063/1.369690.

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YAMAMOTO, A., H. TAKAKURA, and A. P. TSAI. "Refinement of i-Al-Cu-Fe and i-Al-Cu-Ru Quasicrystal Structures." Ferroelectrics 305, no. 1 (January 2004): 279–82. http://dx.doi.org/10.1080/00150190490463026.

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Srivastava, Radhey S., Roy Bertrand, August A. Gallo, and Kenneth M. Nicholas. "Cu(I)/Cu(II)-catalyzed allylic amination of alkenes." Tetrahedron Letters 52, no. 27 (July 2011): 3478–80. http://dx.doi.org/10.1016/j.tetlet.2011.04.119.

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Sugar, Jack, and Arlene Musgrove. "Energy Levels of Copper, Cu I through Cu XXIX." Journal of Physical and Chemical Reference Data 19, no. 3 (May 1990): 527–616. http://dx.doi.org/10.1063/1.555855.

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Saha, Subrata, and Pradyut Ghosh. "Cu(I)/Cu(II) templated functional pseudorotaxanes and rotaxanes." Journal of Chemical Sciences 124, no. 6 (November 2012): 1229–37. http://dx.doi.org/10.1007/s12039-012-0326-1.

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Movahedi, Alireza, Angelica Lundin, Nina Kann, Magnus Nydén, and Kasper Moth-Poulsen. "Cu(i) stabilizing crosslinked polyethyleneimine." Physical Chemistry Chemical Physics 17, no. 28 (2015): 18327–36. http://dx.doi.org/10.1039/c5cp02198g.

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With the aim to regulate the coordination environment of Cu(i) and Cu(ii) ions, we have prepared a triazole dialdehyde crosslinking agent with ‘soft’ coordination that can crosslink PEIviaindirect reductive amination.
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Dissertations / Theses on the topic "Cu(I)"

1

Uljanionok, Julija. "Cu(I) Kompleksų vaidmuo glicinatinių ir maleatinių Cu(II) kompleksų elektrocheminės redukcijos procesuose." Doctoral thesis, Lithuanian Academic Libraries Network (LABT), 2010. http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2010~D_20100204_100342-68643.

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Atliktas palyginamasis dviejų kompleksinių sistemų - Cu|Cu(II), glicinas ir Cu|Cu(II), maleino rūgštis - elektrocheminių charakteristikų tyrimas. Nustatytos maleino rūgšties tirpalų pusiausvyrinės charakteristikos. Kiekybiniam titravimo kreivių aprašymui išvestos lygtys, kuriose įvertinti medžiagų bei krūvių balansai bei atsižvelgta į praskiedimo efektus. Jų taikymas pH-metrinių duomenų analizei davė tokias maleato anijonų protonizacijos konstantų reikšmes: log = 6,05, log = 7,48. Nustatyta, kad tirpaluose su 0,3 M K2SO4 priedu protonizuotų ligando formų stabilumas sumažėja (log = 5,75, log = 7,30). Cu(II) maleatinių kompleksų stabilumui nustatyti panaudotas spektrofotometrijos metodas ir pasiūlyta duomenų analizės procedūra. Ji remiasi kiekybiniu absorbcijos spektrų aprašymu, taikant lygtis, išplaukiančias iš valdomo harmoninio osciliatoriaus teorijos. Išanalizavus įvairių sudėčių tirpalų absorbcijos maksimumo dydžius, prieita išvados, kad rūgščiose terpėse vyrauja monoligandinis kompleksas, kurio koncentracinė stabilumo konstanta log b1 = 2,2. Atlikta sistemos Cu|Cu(II), maleino rūgštis pusiausvyrų termodinaminė analizė. Nustatyta, kad esant metalinio vario ir tirpalų sąlyčiui, sistemoje galimi gilūs virsmai, kurių metu iki 90 % Cu(II) transformuojasi į Cu(I). Teorines išvadas patvirtina eksperimentiniai duomenys, gauti spektrofotometrijos ir elektrocheminės kvarco kristalo mikrogravimetrijos metodais. Įvertinti Cu korozijos bei fazinių Cu2O sluoksnių susidarymo... [toliau žr. visą tekstą]
A comparative investigation of electrochemical characteristics of two complex systems, viz. Cu|Cu(II), glycine and Cu|Cu(II), maleic acid, was carried out. The equations were obtained for quantitative description of pH-metric and spectrophotometric data, which were used for determination of equilibrium characteristics in Cu(II)-maleic acid solutions. Thermodynamic analysis shows that deep changes are possible in this system resulting in 90 % transform of Cu(II) into Cu(I). The rates of Cu corrosion and Cu2O formation are estimated to be of the same order (nmol cm-2 s-1). Regularities of formal electrochemical kinetics, which account for the mass transport of chemically interacting particles and for step-wise charge transfer process, are suitable for interpretation of voltammetric data of the Cu|Cu(II), glycine system. Kinetic parameters Cu(II) glycinate complex depend on the nature of the supporting electrolyte: the exchange current density decreases and the cathodic charge transfer coefficient increases in the sequence: Li+ - Na+ - K+ - Cs+. To enhance the Cu(I) generation in maleic acid system, the pre-electrolysis procedure was applied. It was found that its effect depends on solution pH. Applied theoretical model describes satisfactorily the steady-state voltammetric characteristics of Cu|Cu(II), maleic acid system, but some contradictory results were obtained in the case of time-dependent processes. Theoretical and experimental problems to be solved are discussed.
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Dolderer, Benedikt. "Zur molekularen Architektur von Cu(I)-Thiolatzentren in Cu-Thioneinen." [S.l. : s.n.], 2004. http://deposit.ddb.de/cgi-bin/dokserv?idn=973266295.

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Uljanionok, Julija. "Role of Cu(I) complexes in the electrochemical reduction of glycinate and maleate Cu(II) complexes." Doctoral thesis, Lithuanian Academic Libraries Network (LABT), 2010. http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2010~D_20100204_100357-81350.

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A comparative investigation of electrochemical characteristics of two complex systems, viz. Cu|Cu(II), glycine and Cu|Cu(II), maleic acid, was carried out. The equations were obtained for quantitative description of pH-metric and spectrophotometric data, which were used for determination of equilibrium characteristics in Cu(II)-maleic acid solutions. Thermodynamic analysis shows that deep changes are possible in this system resulting in 90 % transform of Cu(II) into Cu(I). The rates of Cu corrosion and Cu2O formation are estimated to be of the same order (nmol cm-2 s-1). Regularities of formal electrochemical kinetics, which account for the mass transport of chemically interacting particles and for step-wise charge transfer process, are suitable for interpretation of voltammetric data of the Cu|Cu(II), glycine system. Kinetic parameters Cu(II) glycinate complex depend on the nature of the supporting electrolyte: the exchange current density decreases and the cathodic charge transfer coefficient increases in the sequence: Li+ - Na+ - K+ - Cs+. To enhance the Cu(I) generation in maleic acid system, the pre-electrolysis procedure was applied. It was found that its effect depends on solution pH. Applied theoretical model describes satisfactorily the steady-state voltammetric characteristics of Cu|Cu(II), maleic acid system, but some contradictory results were obtained in the case of time-dependent processes. Theoretical and experimental problems to be solved are discussed.
Atliktas palyginamasis dviejų kompleksinių sistemų - Cu|Cu(II), glicinas ir Cu|Cu(II), maleino rūgštis - elektrocheminių charakteristikų tyrimas. Nustatytos maleino rūgšties tirpalų pusiausvyrinės charakteristikos. Kiekybiniam titravimo kreivių aprašymui išvestos lygtys, kuriose įvertinti medžiagų bei krūvių balansai bei atsižvelgta į praskiedimo efektus. Jų taikymas pH-metrinių duomenų analizei davė tokias maleato anijonų protonizacijos konstantų reikšmes: log = 6,05, log = 7,48. Nustatyta, kad tirpaluose su 0,3 M K2SO4 priedu protonizuotų ligando formų stabilumas sumažėja (log = 5,75, log = 7,30). Cu(II) maleatinių kompleksų stabilumui nustatyti panaudotas spektrofotometrijos metodas ir pasiūlyta duomenų analizės procedūra. Ji remiasi kiekybiniu absorbcijos spektrų aprašymu, taikant lygtis, išplaukiančias iš valdomo harmoninio osciliatoriaus teorijos. Išanalizavus įvairių sudėčių tirpalų absorbcijos maksimumo dydžius, prieita išvados, kad rūgščiose terpėse vyrauja monoligandinis kompleksas, kurio koncentracinė stabilumo konstanta log b1 = 2,2. Atlikta sistemos Cu|Cu(II), maleino rūgštis pusiausvyrų termodinaminė analizė. Nustatyta, kad esant metalinio vario ir tirpalų sąlyčiui, sistemoje galimi gilūs virsmai, kurių metu iki 90 % Cu(II) transformuojasi į Cu(I). Teorines išvadas patvirtina eksperimentiniai duomenys, gauti spektrofotometrijos ir elektrocheminės kvarco kristalo mikrogravimetrijos metodais. Įvertinti Cu korozijos bei fazinių Cu2O sluoksnių susidarymo... [toliau žr. visą tekstą]
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4

Robin, Adeline. "Structural diversity of Cu(I), Ag(I) and Cu(II) coordination polymers with the ligand ethanediyl bis(isonicotinate) /." Basel : [s.n.], 2005. http://edoc.unibas.ch/diss/DissB_7305.

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5

Moustafa, Khalil Ali. "Assemblages Polymétalliques Luminescents de L'ion Cu(I)." Thesis, Rennes, INSA, 2019. http://www.theses.fr/2019ISAR0018.

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Ce manuscrit décrit en détail la réactivité du précurseur pré-organisé A 1 de formule [Cu 2 (μ 2 - dppm) 2 (CN) 2 ].(PF 6 ) 2 , basé sur des ions de Cu(I) avec différents types de ligands afin de synthétiser de nouveaux assemblages polymétalliques luminescent. Cette réactivité utilise pleinement les concepts de chimie supramoléculaire guidée par la chimie de coordination (CDS), ce qui permet d’obtenir un grand nombre d’assemblages supramoléculaires polymétalliques complexes et variés de l’ion Cu(I). Ils sont obtenus à partir de synthèses simples et présentent une grande variété de caractéristiques structurales. Sur la base de ce résultat, nous sommes intéressés de voir dans quelle mesure il est possible d’étendre l’approche synthétique originale de chimie supramoléculaire adaptative guidée par la coordination développée au laboratoire à l’utilisation de précurseurs présentant des fragments cyano, tels que les fragments K 2 M(CN) 4 (M= Ni, Pd, Pt), K 2 Pt(CN) 6 , K 4 M(CN) 8 (M= Mo et W) et des précurseurs inorganiques anioniques qui ne présentent pas de centre métallique,tels que le KC(CN) 3 , le NaN(CN) 2 et le NaN 3 . Dans le dernier chapitre, le dérivé A 1 a été mis à réagir avec des ligands polytopiques à terminaison pyridine ce qui a permis de caractériser de nouveaux polymères de coordination. Les nouveaux dérivés sont caractérisés en utilisant différentes techniques comme la RMN multinucléaire, des études de diffraction des rayons X sur monocristaux et sur poudre, les spectroscopies UV-Vis et IR. En outre, les propriétés photophysiques (spectre d'émission, mesures des rendements quantiques et des temps de vie des états excités) des matières émissives obtenues ont été étudiées en solution et à l'état solide à température ambiante et à basse température
This manuscript describes in detail the reactivity of the pre-organized precursor A 1 , whose molecular formula is [Cu 2 (μ 2 -dppm) 2 (CN) 2 ](PF 6 ) 2 , based on Cu(I) ions with different types of ligands in order to synthesize new luminescent polymetallic assemblies. Its reactivity makes full use of the concepts of supramolecular chemistry guided by coordination chemistry (CDS), which makes it possible to obtain a large intricate number and varied polymetallic supramolecular assemblies of the Cu(I) ion. They are obtained from simple syntheses and with a wide variety of structural characteristics. Based on this result, we are interested to see how it is possible to extend the original adaptive coordination driven supramolecular approach developed in our group to the use of precursors bearing cyano fragments, such as K 2 M(CN) 4 (M= Ni, Pd, Pt), K 2 Pt(CN) 6 , K 4 M(CN) 8 (M= Mo and W) and also anionic inorganic precursors that do not have a metal centre, such as KC(CN) 3 , NaN(CN) 2 and NaN 3 .In the last chapter, the A 1 derivative has been reacted with pyridine- terminated polytopic ligands, which has made it possible to characterize novel coordination polymers. The new derivatives are characterized using different techniques such as multinuclear NMR, single-crystal and powder X-ray diffraction studies, UV-Vis and IR spectroscopies. In addition, the photophysical properties (emission spectrum, measurements of quantum yields and life times of the excited states) of the emissive materials obtained have been studied in solution and in the solid state at room temperature and at low temperature
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Michaels, Hannes. "Cu(I)/(II) mixed-valence Coordination Polymers." Thesis, Uppsala universitet, Institutionen för fysik och astronomi, 2017. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-330861.

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Morgan, Dieisson. "Síntese e caracterização de complexos de Cu(I), Cu(II) E Au(I) com ligantes triazenidos contendo substituintes triazóis." Universidade Federal de Santa Maria, 2013. http://repositorio.ufsm.br/handle/1/10563.

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Triazenido ions are isoelectronic to amidinato anions,[R'N C(R)=NR']- and have a broad versatility in coordination chemistry. Metal complexes including triazenido ligands find applications in various areas of chemistry. Triazenes and complexes including triazole derivatives show extensive applicability as for example in supramolecular chemistry and pharmacological compounds. This work presents deals with the study of new triazene derivatives with triazole substituents resulting from the click reactions, acting as ligands in complexes with Cu(I), Cu(II) and Au(I). The following ligands 1,3-bis(2-azidophenyl)triazene (2), 1-(methyl)-3-(2-(4-phenyl-1,2,3-triazole)triazene-N-oxide (4), 1-(phenyl)-3-(2-(4-phenyl-1,2,3-triazole)triazene (5), 1,3-bis(2-(4-phenyl-1,2,3-triazole)triazene (6) and, complexes 1,3-bis(2-azidophenyl)triazenide-κN11- triphenylphosphine-gold(I) (2a), bis-{1-(methyl)-3-[2-(4-phenyl-1,2,3-triazole-κN2)]triazenide-1-oxide-κ2N3,O}copper(II) (4b), 1-(phenyl)-3-(2-(4-phenyl-1,2,3-triazole)triazenide-κN- triphenylphosphine-κP-gold(I) (5a), 1,3-bis(2-(4-phenyl-1,2,3-triazole)triazenide-κN- triphenylphosphine-κP-gold(I) (6a), bis[1,3-bis(2-(4-phenyl-1,2,3-triazole-κN2)-μ-N3-triazenide]-κN11,κN13 copper(I)κN13,κN11´copper(I) (Cu Cu) (6b) were investigated. The compounds were characterized by IR, UV-Vis and NMR (1H e 13C) spectroscopy, low or high resolution mass spectrometry (EI, ESI, ESI(+)-TOF and ESI(-)-TOF) and X-ray diffraction on single crystal. Triazene (2) and complex (2a) exhibit intramolecular assembling through classical and non-classical hydrogen bonding. Complexes with Au(I), (2a), (5a) e (6a), the metal atom show linear coordination geometry. The metal atom in complex (6b) shows a T distorted coordination geometry, which is extended to a quadratic coordination resulting from d10 d10 interactions between Cu(I) ions. Triazene (6) and its respective complexes (6a) e (6b) exhibit intermolecular interactions of the type C−H···M. Antibacterial activity of triazene (5) and complex (5a) were assayed resulting to be inactive against the bacteria tested.
Os compostos triazenidos são isoeletrônicos a íons amidinatos [R'NH C(R)=NR'], e têm sido usados com sucesso na química de coordenação. A complexação a íons metálicos possibilita a sua aplicação em diversas áreas da química. Assim como os triazenos, os triazóis possuem vasta aplicabilidade, desde a química supramolecular até a área farmacológica. Este trabalho apresenta o estudo inédito de pré-ligantes triazenos contendo substituintes triazóis os quais foram obtidos a partir de reações de Click, e seus respectivos complexos de Cu(I), Cu(II) e Au(I). Foram sintetizados os pré-ligantes 1,3-bis(2-azidofenil)triazeno (2), 1-(metil)-3-(2-(4-fenil-1,2,3-triazol)triazeno-N-óxido (4), 1-(fenil)-3-(2-(4-fenil-1,2,3-triazol)triazeno (5), 1,3-bis(2-(4-fenil-1,2,3-triazol)triazeno (6) e os complexos 1,3-bis(2-azidofenil)triazenido-κN11-trifenilfosfina-ouro(I) (2a), bis-{1-(metil)-3-[2-(4-fenil-1,2,3-triazol-κN2)]triazenido-1-óxido-κ2N3,O}cobre(II) (4b), 1-(fenil)-3-(2-(4-fenil-1,2,3-triazol)triazenido-κN-trifenilfosfina-κP-ouro(I) (5a), 1,3-bis(2-(4-fenil-1,2,3-triazol)triazenido-κN-trifenilfosfina-κP-ouro(I) (6a), bis[1,3-bis(2-(4-fenil-1,2,3-triazol-κN2)-μ-N3-triazenido]-κN11,κN13 - cobre(I)κN13,κN11´cobre(I) (Cu Cu) (6b). Estes foram caracterizados por espectroscopia de IV, UV-Vis e RMN (1H e 13C), espectrometria de massas de baixa ou alta resolução (EI, ESI, ESI(+)-TOF e ESI(-)-TOF) e difração de raios X em monocristal. O triazeno (2) e complexo (2a) apresentam ligações de hidrogênio intermoleculares e intramoleculares do tipo clássica e não-clássica. Os complexos de Au(I), (2a), (5a) e (6a) possuem geometria de coordenação linear. O complexo (6b) apresenta uma geometria T distorcida, a qual é estendida para quadrática pela interação d10 d10 entre os átomos de Cu(I), o triazeno (6) e seus complexos (6a) e (6b) apresentam ainda ligações intermoleculares do tipo C−H···M. Foi testada a atividade antibacteriana do triazeno (5) e o complexo (5a), os quais mostraram-se inativos frente às bactérias testadas.
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GUIMARÃES, JÚNIOR Walber Gonçalves. "Estudo Teórico da Adsorção de Gases Leves nas Redes Metalorgânicas SIFSIX-2-Cu, SIFSIX-2-Cu-i e SIFSIX-3-Cu." reponame:Repositório Institucional da UNIFEI, 2017. http://repositorio.unifei.edu.br:8080/xmlui/handle/123456789/807.

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Submitted by repositorio repositorio (repositorio@unifei.edu.br) on 2017-06-14T12:21:00Z No. of bitstreams: 1 dissertacao_guimaraes_junior_2017.pdf: 4205944 bytes, checksum: 790534ecbec8c030d09e742ba01b318b (MD5)
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O dióxido de carbono, assim como outros gases leves denominados gases estufa, afetam de maneira negativa o sistema de temperatura global, agravando o efeito estufa desde a primeira revolução industrial. Mesmo a concentração nunca ter sido constante, a atividade antropogênica fez com que concentração desses gases na atmosfera aumentar de maneira exponencial. Por essa razão, países adotam estratégias para reduzir a concentração desses gases na atmosfera. O sequestro e captura de gases mostrou-se ser uma medida promissora na redução de gases estufa. O uso de alcanoaminas foi de grande relevância nesse processo, porém seu custo de reciclagem foi se elevando ao ponto de ser um material inviável para a adsorção de gases estufa, em especial o CO₂ devido sua quantidade. A utilização de redes metalorgânicas, materiais híbridos que sua topologia consiste em ligantes orgânicos coordenados a nós metálicos. Esses materiais de alta porosidade e grande área superficial aumentou o interesse em diversos campos de estudo, desde a catalise heterogênea até o transporte controlado de fármacos. Em 1999, Omar Yaghi utilizou esses materiais para a adsorção seletiva de gases, com foco em CO₂. Recentemente, a família SIFSIX se mostrou promissora na captura seletiva de CO₂, utilizando de unidades orgânicas de 1,2-di(piridin-4-il)etino e pilares inorgânicos a base de SiF₆²⁻. Nessa família, as redes metalorgânicas SIFSIX-2-Cu, SIFSIX-2-Cu-i e SIFSIX-3-Cu mostraram-se capazes de realizar a adsorção seletiva de CO₂ com uma alta capacidade em relação as suas concorrentes. A estrutura SIFSIX-3-Cu é a atual recordista de captura seletiva de CO₂. Por isso, o mecanismo de adsorção para gases leves é investigado utilizando-se DFT. A adsorção dos gases CH₄, CO₂, CO, H₂, N₂ e O₂ nas redes metalorgânicas SIFSIX-2-Cu, SIFSIX-2-Cu-i e SIFSIX-3-Cu foi estudada, afim de se entender o processo de adsorção dessa família. Resultados indicam a seletividade do CO₂ ser produto de seu alto momento de quadrupolo, onde o grupo aniônico, SiF₆²⁻, teve um papel importante para a adsorção.
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Mazzanti, Francesco. "Studio dell'intorno locale di complessi antitumorali di Cu(I) e (II) tramite spettroscopia di assorbimento X." Master's thesis, Alma Mater Studiorum - Università di Bologna, 2015. http://amslaurea.unibo.it/9308/.

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In questo lavoro è presentato l'utilizzo della spettroscopia di assorbimento di raggi X applicata all'indagine inerente il numero e la natura degli atomi vicini di un centro metallico a due diversi stati di ossidazione [Cu(I) e Cu(II)] all'interno di complessi fosfinici e/o azotati. Gli spettri sono stati registrati nella loro completezza, comprendendo sia la soglia sia lo spettro esteso di assorbimento, e le transizioni elettroniche 1s→3d e 1s→4p sono state oggetto d'esame per avere indicazioni circa l'intorno locale del fotoassorbitore (l'atomo centrale). La tecnica più utilizzata, tuttavia, è stata l'analisi EXAFS (Extended X-ray Absorption Fine Structure) che ha permesso di determinare l’effettiva coordinazione di Cu(I) e (II) nel caso dei complessi studiati. Il metodo consiste nella costruzione di un segnale teorico più simile possibile a quello ottenuto sperimentalmente, e l’approccio per raggiungere questo obiettivo consiste nel seguire una procedura di fitting eseguita computazionalmente (tramite il pacchetto software GNXAS), per la quale è necessario un modello strutturale già esistente o creato ex novo da una molecola di partenza molto simile. Sarà presentato lo studio degli esperimenti ottenuti su campioni sia solidi che in soluzione: in questo modo è stato possibile effettuare un confronto tra le due forme dello stesso composto nonché si è potuto osservare i cambiamenti riguardanti l’interazione metallo-solvente a diverse concentrazioni. Come sarà mostrato in seguito, l’analisi sui solidi è risultata più affidabile rispetto a quella riferita alle soluzioni; infatti il basso rapporto segnale/rumore caratterizzante le misure di queste ultime ha limitato le informazioni ottenibili dai relativi spettri di assorbimento di raggi X.
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Bassan, David Michael [Verfasser]. "Cu(I) catalyzed reaction of hydroxylamines / David Michael Bassan." Gießen : Universitätsbibliothek, 2016. http://d-nb.info/1081627492/34.

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Books on the topic "Cu(I)"

1

Michael. Convorbiri cu Mihai I al României. București: Humanitas, 1991.

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Gheo, Radu Pavel. Adio, adio, patria mea cu î din i, cu â din a. Iași: Polirom, 2003.

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Michael. Noi convorbiri cu Mihai I al României. București: Humanitas, 1992.

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Philippide, Alexandru I. Alexandru I. Philippide în dialog cu contemporanii: Documente literare. București: Minerva, 1986.

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Philippide, Alexandru I. Alexandru I. Philippide în dialog cu contemporanii: Documente literare. București: Minerva, 1986.

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Bucov, Emilian. Mi-i dor de țara cu cireși: Poezii și poeme. Chișinău: Lumina, 2005.

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Michael. În fața neamului meu: Convorbiri cu Mihai I al României. Iași: Editura Princeps, 1995.

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Harutyunyan, Syuzanna R., ed. Progress in Enantioselective Cu(I)-catalyzed Formation of Stereogenic Centers. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-33414-1.

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Muscarà, Sarah Zappulla. Odissea di maschere: 'A birritta cu 'i ciancianeddi di Luigi Pirandello. Cantania: G. Maimone, 1988.

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Codul cu privire la locuințe al Republicii Moldova: Cu ultimile modificări și completări = Zhilishchnyĭ kodeks Respubliki Moldova : s poslednimi izmenenii︠a︡mi i dopolnenii︠a︡mi. Chișinău: "Lavilat-Info" SRL, 2011.

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Book chapters on the topic "Cu(I)"

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Tsuboyama, Akira. "Luminescent Dinuclear Copper(I) Complexes with Short Intramolecular Cu-Cu Distances." In Highly Efficient OLEDs, 93–118. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2018. http://dx.doi.org/10.1002/9783527691722.ch3.

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Macdougall, Jennie, Chris Reid, and Larry McGhee. "Implications of the Selectiveness of Cu Chelators on Cu0, Cu(I)O and Cu(II)O Powders." In Solid State Phenomena, 329–32. Stafa: Trans Tech Publications Ltd., 2007. http://dx.doi.org/10.4028/3-908451-46-9.329.

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Joost, Maximilian. "Copper: σ-SiH Coordination to Cu(I)." In Synthesis and Original Reactivity of Copper and Gold Complexes, 5–29. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-18690-0_2.

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Oshio, H., and T. Ito. "Assembly of Imino Nitroxides with Cu(I) Halides." In ACS Symposium Series, 266–75. Washington, DC: American Chemical Society, 1996. http://dx.doi.org/10.1021/bk-1996-0644.ch018.

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Beltramini, M., K. Münger, U. A. Germann, and Konrad Lerch. "Luminescence Emission from the Cu(I)-Thiolate Complex in Metallothioneins." In Experientia Supplementum, 237–41. Basel: Birkhäuser Basel, 1987. http://dx.doi.org/10.1007/978-3-0348-6784-9_17.

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Wei, Xiaofeng, Yohei Shimizu, and Motomu Kanai. "Catalytic Asymmetric Addition Reactions of Cu(I)-Conjugated Soft Carbon Nucleophiles." In Progress in Enantioselective Cu(I)-catalyzed Formation of Stereogenic Centers, 169–82. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/3418_2015_163.

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Hensel, Alexander, and Martin Oestreich. "Asymmetric Addition of Boron and Silicon Nucleophiles." In Progress in Enantioselective Cu(I)-catalyzed Formation of Stereogenic Centers, 135–67. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/3418_2015_156.

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Malkov, Andrei V., and Kurt Lawson. "1,2- Versus 1,4-Asymmetric Reduction of Ketones." In Progress in Enantioselective Cu(I)-catalyzed Formation of Stereogenic Centers, 207–20. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/3418_2015_157.

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Maciá, Beatriz. "Formation of Quaternary Stereocentres by Copper-Catalysed Enantioselective Conjugate Addition Reaction." In Progress in Enantioselective Cu(I)-catalyzed Formation of Stereogenic Centers, 41–98. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/3418_2015_158.

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Fang, Xin, Jia-Wei Zhang, and Chun-Jiang Wang. "Asymmetric Cycloaddition and Cascade Addition–Cyclization Reactions." In Progress in Enantioselective Cu(I)-catalyzed Formation of Stereogenic Centers, 183–205. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/3418_2015_160.

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Conference papers on the topic "Cu(I)"

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Kurooka, Shunji, Yoshinori Hotta, Ai Nakamura, Mitsumasa Koyanagi, and Takahumi Fukushima. "Cu-Cu Bonding Challenges with ‘i-ACF’ for Advanced 3D Integration." In 2019 International 3D Systems Integration Conference (3DIC). IEEE, 2019. http://dx.doi.org/10.1109/3dic48104.2019.9058773.

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Tobin, Rod C., Alfred K. Anders, Erol C. Harvey, and Stuart C. Rae. "Characterization Of Sputtering-Based Unheated Cu I And Au I Lasers." In OE/LASE '89, edited by Jin J. Kim, Randy Kimball, and P. J. Wisoff. SPIE, 1989. http://dx.doi.org/10.1117/12.951227.

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Milašinović, Veljko, Sergii Voinarovych, Karlo Raić, Krysztof Krasnowski, Nenad Radović, Ana Alil, and Bojan Gligorijević. "Uticaj početne dužine Cu šipki na strukturu i mikro-tvrdoću frikciono zavarenih i presovanih Al/Cu bimetalnih spojeva." In 31st International Congress on Process Industry. Union of Mechanical and Electrotechnical Engineers and Technicians of Serbia, 2018. http://dx.doi.org/10.24094/ptk.018.31.1.187.

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Michaels, Hannes. "Highly-stable Cu(I)/(II) oxazoline-bipyridine complexes." In 10th International Conference on Hybrid and Organic Photovoltaics. Valencia: Fundació Scito, 2018. http://dx.doi.org/10.29363/nanoge.hopv.2018.072.

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Xu, Shuang, J. Weber, and Casey Christopher. "UV SPECTROSCOPY ON GAS PHASE Cu(I)-BIPYRIDYL COMPLEXES." In 70th International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2015. http://dx.doi.org/10.15278/isms.2015.ta09.

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Lyubovskava, R. N., M. Z. Aldoshina, V. A. Konovalikhin, O. A. Dyachenko, and R. B. Lyubovskii. "ET salt with [Cu(I)Hg(II)] containing anion." In International Conference on Science and Technology of Synthetic Metals. IEEE, 1994. http://dx.doi.org/10.1109/stsm.1994.834903.

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Bahari, Z., F. Thévet, J. Rivet, and J. Dugué. "Contribution à l’étude expérimentale du système ternaire Bi-Cu-I : Description du triangle CuI-BiI3-I." In XXXV JEEP – 35th Conference on Phase Equilibria. Les Ulis, France: EDP Sciences, 2009. http://dx.doi.org/10.1051/jeep/200900020.

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"Atomnaya relaksatsiya i vibratsionnye svoystva malykh metallicheskikh klasterov na poverkhnosti Cu(111)." In Perspektivnye materialy s ierarkhicheskoy strukturoy dlya novykh tekhnologiy i nadezhnykh konstruktsiy, Khimiya nefti i gaza. Tomsk State University, 2018. http://dx.doi.org/10.17223/9785946217408/121.

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Dyubko, S. F., V. A. Efremov, V. G. Gerasimov, M. N. Efimenko, M. P. Perepechay, and K. B. MacAdam. "Laser-microwave spectroscopy of Cu I atoms in S Rydberg state." In 2008 International Conference on Advanced Optoelectronics and Lasers (CAOL). IEEE, 2008. http://dx.doi.org/10.1109/caol.2008.4671875.

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Gašparová, Renata, Mária Maliarová, Tatiana Ďurčeková, Filip Kraic, and Ján Titiš. "Synthesis of furo[3,2-b]pyrrole-5-carboxhydrazides and Their Cu, Ni and Co Complexes." In The 15th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2011. http://dx.doi.org/10.3390/ecsoc-15-00568.

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Reports on the topic "Cu(I)"

1

Maggard, Paul A. Photoelectrochemistry, Electronic Structure, and Bandgap Sizes of Semiconducting Cu(I)-Niobates and Cu(I)-Tantalates. Office of Scientific and Technical Information (OSTI), November 2013. http://dx.doi.org/10.2172/1105011.

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Ross, M., R. Boehler, and D. Errandonea. Melting of transition metals at high pressure and the influence of liquid frustration. I. The late metals Cu, Ni and Fe. Office of Scientific and Technical Information (OSTI), March 2007. http://dx.doi.org/10.2172/908119.

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Fawcett, W. R., Colby A. Foss, and Jr. Solvent Donicity and Dielectric Continuum Effects in Amalgam Formation Reactions. A Study of the Reduction of Cu(I) in the Nitrile Solvents. Fort Belvoir, VA: Defense Technical Information Center, May 1991. http://dx.doi.org/10.21236/ada237239.

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