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Journal articles on the topic 'Cu(I)'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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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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2

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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3

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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5

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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6

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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7

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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8

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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9

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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10

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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11

Chen, Yong, Jun-Li Li, Glenna So Ming Tong, Wei Lu, Wen-Fu Fu, Siu-Wai Lai, and Chi-Ming Che. "Nanostructures of tetranuclear copper(i) complexes with short Cu(i)⋯Cu(i) contacts: crystallization-induced emission enhancement." Chemical Science 2, no. 8 (2011): 1509. http://dx.doi.org/10.1039/c0sc00597e.

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12

Saeedifard, Farzaneh, M. Thomas Morgan, John Bacsa, and Christoph J. Fahrni. "Preorganized PSP Ligands Yield Monomeric Cu(I) Complexes with Subzeptomolar Cu(I) Dissociation Constants." Inorganic Chemistry 58, no. 20 (May 24, 2019): 13631–38. http://dx.doi.org/10.1021/acs.inorgchem.9b00965.

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13

BENAZETH, S., M. DANOT, P. COLOMBET, H. DEXPERT, and P. LAGARDE. "EVIDENCE FOR SHORT Cu(I)-Cu(I) DISTANCES IN COPPER-EXCESS SPINELS FROM EXAFS." Le Journal de Physique Colloques 47, no. C8 (December 1986): C8–777—C8–780. http://dx.doi.org/10.1051/jphyscol:19868148.

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14

Altiparmak, Ismihan, Busra Karakaya, Deniz Uner, and Bahar Ipek. "H2 adsorption on Cu(I)-ZSM-5: Exploration of Cu(I)-exchange in solution." International Journal of Hydrogen Energy 44, no. 34 (July 2019): 18866–74. http://dx.doi.org/10.1016/j.ijhydene.2018.10.111.

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15

Kishore, Pilli V. V. N., Jian-Hong Liao, Hsing-Nan Hou, Yan-Ru Lin, and C. W. Liu. "Ferrocene-Functionalized Cu(I)/Ag(I) Dithiocarbamate Clusters." Inorganic Chemistry 55, no. 7 (March 24, 2016): 3663–73. http://dx.doi.org/10.1021/acs.inorgchem.6b00201.

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16

Xiao, Chang, and Song-Lin Zhang. "Isolation of OH-bridged Ag(i)/Cu(iii) and ion-pair Cu(i)/Cu(iii) trifluoromethyl complexes with monophosphines." Dalton Transactions 48, no. 3 (2019): 848–53. http://dx.doi.org/10.1039/c8dt03876g.

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17

Nishikawa, Michihiro, Taichi Sano, Masaya Washimi, Koichiro Takao, and Taro Tsubomura. "Emission properties and Cu(i)–Cu(i) interaction in 2-coordinate dicopper(i)-bis(N-heterocyclic)carbene complexes." Dalton Transactions 45, no. 30 (2016): 12127–36. http://dx.doi.org/10.1039/c6dt01239f.

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The 8-shaped dinuclear copper(i) complexes bearing two N-heterocyclic carbene ligands exhibit strong photoluminescence both in solution and the solid states. Copper(i)–copper(i) interactions play a key role in the photophysical properties.

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18

Bazán, Julio C., Gabriela M. Lescano, María R. Prat, and Aurora Sagua. "Reduction of Cu(II) to Cu(I) in solid CsCuCl3." Materials Chemistry and Physics 125, no. 3 (February 2011): 542–47. http://dx.doi.org/10.1016/j.matchemphys.2010.10.019.

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19

Harding, Charlie, Vickie McKee, and Jane Nelson. "Highly delocalized Cu(I)/Cu(II); a copper-copper bond?" Journal of the American Chemical Society 113, no. 25 (December 1991): 9684–85. http://dx.doi.org/10.1021/ja00025a050.

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20

Pike, Robert D., Gerardo Ayala, and Alba P. Evans. "Cu(I)···H–C Bonding in Cu(2,3-Diphenylquinoxaline)ClO4." Journal of Chemical Crystallography 44, no. 10 (September 20, 2014): 520–26. http://dx.doi.org/10.1007/s10870-014-0545-z.

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21

Lu, Taotao, Jin-Yun Wang, Lin-Xi Shi, Zhong-Ning Chen, Xue-Tai Chen, and Zi-Ling Xue. "Synthesis, structures and luminescence properties of amine-bis(N-heterocyclic carbene) copper(i) and silver(i) complexes." Dalton Transactions 47, no. 19 (2018): 6742–53. http://dx.doi.org/10.1039/c8dt00599k.

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Mononuclear Ag(i), Cu(i) and heterometallic Cu(i)/Ag(i) complexes with the tridentate amine-bis(N-heterocyclic carbene) were prepared, among which Cu(i)- and Cu/Ag complexes show luminescence properties.

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22

Nagai, Hiroki, Tatsuya Suzuki, Chihiro Mochizuki, Ichiro Takano Tohru Honda, and Mitsunobu Sato. "Formation Mechanism of p-Type Cu₂O Thin Films via Intermediate Cu⁰ Species Derived from Cu(II) Complex of Ethylenediamine-N,N,N′,N′-Tetraacetic Acid." Science of Advanced Materials 6, no. 3 (March 1, 2014): 603–11. http://dx.doi.org/10.1166/sam.2014.1788.

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23

Himoto, K., S. Suzuki, T. Okubo, M. Maekawa, and T. Kuroda-Sowa. "A new semiconducting 1D Cu(i)–Cu(ii) mixed-valence coordination polymer with Cu(ii) dimethylpiperidine–dithiocarbamate and a tetranuclear Cu(i)–Br cluster unit." New Journal of Chemistry 42, no. 6 (2018): 3995–98. http://dx.doi.org/10.1039/c7nj04763k.

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24

Oshio, Hiroki, Takashi Watanabe, Akihiro Ohto, Tasuku Ito, Tadaaki Ikoma, and Shozo Tero-kubota. "Magnetic Interactions in Cu(I) and Ag(I) Iminonitroxides." Molecular Crystals and Liquid Crystals Science and Technology. Section A. Molecular Crystals and Liquid Crystals 273, no. 1 (November 1995): 47–56. http://dx.doi.org/10.1080/10587259508031841.

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25

Yarykin, Nikolai, and Jörg Weber. "Metastable CuVO* Complex in Silicon." Solid State Phenomena 205-206 (October 2013): 255–59. http://dx.doi.org/10.4028/www.scientific.net/ssp.205-206.255.

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The reaction of the mobile interstitial Cui atom and the A-center (vacancy-oxygen complex) was recently reported to produce at 350 K the rather stable CuVO complex. Chemomechanical polishing in a copper-contaminated slurry allowed to lower the copper in-diffusion temperature down to 295K. The development of the CuVO complex is shown to proceed via formation of the metastable precursor (CuVO*) which introduces two deep levels in the lower half of the band gap. The CuVO* defect is unstable at room temperature and transforms completely into the CuVO complex by a 30 min anneal at 350 K. The proposed structure for the CuVO* complex of a Cui atom trapped nearby the A-center is supported by recent ab-initio calculations.

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26

Holzner, C. "Lumineszierende Cu(I)- und Ag(I)-Cluster mit Thionoliganden." Monatshefte f�r Chemie Chemical Monthly 125, no. 12 (December 1994): 1353–64. http://dx.doi.org/10.1007/bf00811084.

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27

MUELLER, J. F. K., and P. VOGT. "ChemInform Abstract: Cu(I)-Catalyzed Sulfoximination." ChemInform 29, no. 38 (June 19, 2010): no. http://dx.doi.org/10.1002/chin.199838092.

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28

Zhao, Baoguo, Haifeng Du, and Yian Shi. "Cu(I)-Catalyzed Cycloguanidination of Olefins." Organic Letters 10, no. 6 (March 2008): 1087–90. http://dx.doi.org/10.1021/ol702974s.

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29

Pong, Ian, Christian Scheuerlein, Carmine Senatore, Ludovic Thilly, Marco Di Michiel, Alexandre Gerardin, Simon C. Hopkins, et al. "Cu Ti Formation in Nb Ti/Cu Superconducting Strand Monitored by In Situ Techniques." Defect and Diffusion Forum 297-301 (April 2010): 695–701. http://dx.doi.org/10.4028/www.scientific.net/ddf.297-301.695.

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In order to investigate the high temperature exposure effect on Nb Ti/Cu superconducting strands, as might be encountered in joining by soldering and in cabling annealing, X-ray diffraction and resistometry measurements were performed in situ during heat treatment, and complemented by conventional metallography, mechanical tests and superconducting properties measurements. Changes of the Nb Ti nanostructure at temperatures above 300°C are manifested in the degradation of critical current in an applied external magnetic field, although degradation at self field was insignificant up to 400°C for several minutes. Above 500°C, the formation of various Cu Ti intermetallic compounds, due to Ti diffusion from Nb Ti into Cu, is detected by in situ XRD albeit not resolvable by SEM-EDS. There is a ductile to brittle transition near 600°C, and liquid formation is observed below 900°C. The formation of Cu Ti causes a delayed reduction of the residual resistivity ratio (RRR) and adversely affects the deformation behaviour of the strands.

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30

Santra, Biswajit. "Molecular Rearrangement of Trinuclear Cu(I)-NHC: Synthesis of Mono, Binuclear and Polymeric Cu(I)-NHCs." ChemistrySelect 4, no. 6 (February 11, 2019): 1866–71. http://dx.doi.org/10.1002/slct.201803427.

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31

Chiarella, Gina M., Doris Y. Melgarejo, Alex Rozanski, Pierre Hempte, Lisa M. Perez, Christian Reber, and John P. Fackler Jr. "A short, unsupported Cu(i)⋯Cu(i) interaction, 2.65 Å, in a dinuclear guanidine chloride complex." Chem. Commun. 46, no. 1 (2010): 136–38. http://dx.doi.org/10.1039/b918912b.

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32

Kishore, Pilli V. V. N., De-Ren Shi, Jian-Hong Liao, Arvind K. Gupta, and C. W. Liu. "Synthesis and structural characterization of xanthate ligated hydrido Cu(I) clusters and Cu(I) coordination polymer." Inorganica Chimica Acta 496 (October 2019): 119068. http://dx.doi.org/10.1016/j.ica.2019.119068.

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33

Rizk, Nashwa, Samar Aly, Ayman Eldourghamy, Magda El-Salamony, and Asmaa Hashad. "Synthesis, Characterization of Cu(I) Complex of Thiosemicarbazone Ligand and Antibacterial Activity of Cu(I) Complex." Research Journal of Applied Biotechnology 4, no. 2 (November 1, 2018): 30–38. http://dx.doi.org/10.21608/rjab.2018.106800.

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34

Olejnik, Edyta. "Charakterystyki prądowe układów wielowarstwowych Cu/Ni i Cu/stal (Cr-Ni)." ELEKTRONIKA - KONSTRUKCJE, TECHNOLOGIE, ZASTOSOWANIA 1, no. 9 (September 5, 2015): 83–86. http://dx.doi.org/10.15199/13.2015.9.19.

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35

De Wael, Karolien, Philippe Westbroek, Joost De Strycker, Emmanuel Gasana, and Eduard Temmerman. "Electrochemical detection of Cu(I) and Cu(II) in styrene media." Microchemical Journal 77, no. 1 (May 2004): 85–92. http://dx.doi.org/10.1016/j.microc.2004.01.002.

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36

Li, Congcong, Juan Luo, Qixia Zhang, Jianwei Xie, Jinli Zhang, and Bin Dai. "Cu(II)Cu(I)/AC Catalysts for Gas–Solid Acetylene Dimerization." Industrial & Engineering Chemistry Research 59, no. 1 (December 6, 2019): 110–17. http://dx.doi.org/10.1021/acs.iecr.9b05881.

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37

Zhao, Hong, Zhi-Rong Qu, Qiong Ye, Xi-Sen Wang, Jing Zhang, Ren-Gen Xiong, and Xiao-Zeng You. "An Unusual Mixed-Valence Cu(I)−Cu(II) 3-D Framework." Inorganic Chemistry 43, no. 6 (March 2004): 1813–15. http://dx.doi.org/10.1021/ic034943j.

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38

Zhao, Hong, Zhi-Rong Qu, Qiong Ye, Xi-Sen Wang, Jing Zhang, Ren-Gen Xiong, and Xiao-Zeng You. "An Unusual Mixed-Valence Cu(I)−Cu(II) 3-D Framework." Inorganic Chemistry 43, no. 6 (March 2004): 2220. http://dx.doi.org/10.1021/ic040024x.

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39

Konch, Tukhar Jyoti, Mukesh Sharma, Lanka Satyanarayana, Anil Hazarika, Galla V. Karunakar, and Kusum K. Bania. "Non-Hydrothermal Synthesis of Cu(I)-Microleaves from Cu(II)-Nanorods." ChemistrySelect 1, no. 20 (December 1, 2016): 6606–15. http://dx.doi.org/10.1002/slct.201601271.

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40

Saha, Subrata, and Pradyut Ghosh. "ChemInform Abstract: Cu(I)/Cu(II)-Templated Functional Pseudorotaxanes and Rotaxanes." ChemInform 44, no. 33 (July 25, 2013): no. http://dx.doi.org/10.1002/chin.201333219.

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41

Srivastava, Radhey S., Roy III Bertrand, August A. Gallo, and Kenneth M. Nicholas. "ChemInform Abstract: Cu(I)/Cu(II)-Catalyzed Allylic Amination of Alkenes." ChemInform 42, no. 43 (September 29, 2011): no. http://dx.doi.org/10.1002/chin.201143055.

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42

Shu, Mouhai, Weiyin Sun, Chunying Duan, Youjun Fu, Wenxia Tang, and Wenjian Zhang. "Cu(I) and Cu(II) helical complexes formed with oligobipyridine ligand." Science in China Series B: Chemistry 42, no. 5 (October 1999): 501–10. http://dx.doi.org/10.1007/bf02874273.

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43

Mehra, R. K., and P. Mulchandani. "Glutathione-mediated transfer of Cu(I) into phytochelatins." Biochemical Journal 307, no. 3 (May 1, 1995): 697–705. http://dx.doi.org/10.1042/bj3070697.

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Room temperature luminescence attributable to Cu(I)-thiolate clusters has been used to probe the transfer of Cu(I) from Cu(I)-glutathione complex to rabbit liver thionein-II and plant metal-binding peptides phytochelatins (gamma-Glu-Cys)2Gly, (gamma-Glu-Cys)3Gly and (gamma-Glu-Cys)4Gly. Reconstitutions were also performed using CuC1. The Cu(I)-binding stoichiometry of metallothionein or phytochelatins was generally independent of the Cu(I) donor. However, the luminescence of the reconstituted metallothionein or phytochelatins was higher when Cu(I)-GSH was the donor. This higher luminescence is presumably due to the stabilizing effect of GSH on Cu(I)-thiolate clusters. As expected, 12 Cu(I) ions were bound per molecule of metallothionein. The Cu(I) binding to phytochelatins depended on their chain length; the binding stoichiometries being 1.25, 2.0 and 2.5 for (gamma-Glu-Cys)2Gly, (gamma-Glu-Cys)3Gly and (gamma-Glu-Cys)4Gly respectively at neutral pH. A reduced stoichiometry for the longer phytochelatins was observed at alkaline pH. No GSH was found to associate with phytochelatins by a gel-filtration assay. The Cu(I) binding to (gamma-Glu-Cys)2Gly and (gamma-Glu-Cys)3Gly occurred in a biphasic manner in the sense that the relative luminescence increased approximately linearly with the amount of Cu(I) up to a certain molar ratio whereafter luminescence increased dramatically upon the binding of additional Cu(I). The luminescence intensity declined once the metal-binding sites were saturated. In analogy with the studies on metallothioneins, biphasic luminescence suggests the formation of two types of Cu(I) clusters in phytochelatins.

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44

Ferreira, A. M. D. C., M. R. Ciriolo, L. Marcocci, and G. Rotilio. "Copper(I) transfer into metallothionein mediated by glutathione." Biochemical Journal 292, no. 3 (June 15, 1993): 673–76. http://dx.doi.org/10.1042/bj2920673.

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Rabbit liver metallothionein depleted of Cd(II) and Zn(II) was fully reconstituted using a Cu(I)-GSH complex under strictly anaerobic conditions. Anaerobic fluorescence titration, using an emission band at 625 nm which is diagnostic of the correct insertion of Cu(I) into the thiolate clusters of metallothionein, showed that the fluorescence maximum was obtained on addition of as many Cu(I) equivalents as the available Cu(I)-binding sites in the protein (i.e. 12). Binding was nearly complete within 1 min, and Cu(I)-GSH was much more efficient than Cu(I)-thiourea or Cu(I)-acetonitrile in metallothionein reconstitution. In air, full reconstitution was obtained with stoichiometric copper only when an excess of GSH was present in the reaction mixture. Cu(I)-GSH was also able to displace Zn(II) and Cd(II) from natural metallized thionein. It is concluded that: (a) Cu(I)-GSH is a potential physiological Cu(I) carrier, not only for Cu2+/Zn2+ superoxide dismutase [Ciriolo, Desideri, Paci and Rotilio (1990) J. Biol. Chem. 265, 11030-11034] but also for metallothionein; (b) in the case of metallothionein, physiological concentrations of GSH protect the protein from autoxidation in air and facilitate Cu(I)-thiolate exchange; (c) the natural metal composition of metallothionein may be related to metal bioavailability rather than to evolutionary changes in protein structure.

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45

Melnik, Milan. "ChemInform Abstract: Crystallographic Characterization of Four-Coordinate Cu(I), Cu(II) and Cu(III) Complexes." ChemInform 30, no. 48 (June 12, 2010): no. http://dx.doi.org/10.1002/chin.199948270.

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46

Macdougall, Jennie, Chris Reid, and Larry McGhee. "Implications of the Selectiveness of Cu Chelators on Cu⁰, Cu(I)O and Cu(II)O Powders." Solid State Phenomena 134 (November 2007): 329–32. http://dx.doi.org/10.4028/www.scientific.net/ssp.134.329.

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The time and stoichiometric ratio dependence on dissolution of Cu from Cu(I)O and Cu(II)O and metallic Cu was investigated for a series of known Cu chelators. This was monitored by ICP-OES and UV-VIS. A notable difference in the rate of reaction for Cu(I)O vs Cu(II)O was observed and the impact of a copper adduct precipitating from solution discussed as this may present a redeposition issue for Cu surface cleaning. Additionally these chelators were found to selectively favour Cu0 and typically showed higher solution levels of Cu when exposed to the oxides.

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47

Carbonell-Vilar, José M., Elisa Fresta, Donatella Armentano, Rubén D. Costa, Marta Viciano-Chumillas, and Joan Cano. "Photoluminescent Cu(i) vs. Ag(i) complexes: slowing down emission in Cu(i) complexes by pentacoordinate low-lying excited states." Dalton Transactions 48, no. 26 (2019): 9765–75. http://dx.doi.org/10.1039/c9dt00772e.

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48

von Essen, Carolina, Kari Rissanen, and Rakesh Puttreddy. "Halogen Bonds in 2,5-Dihalopyridine-Copper(I) Halide Coordination Polymers." Materials 12, no. 20 (October 11, 2019): 3305. http://dx.doi.org/10.3390/ma12203305.

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Two series of 2,5-dihalopyridine-Cu(I)A (A = I, Br) complexes based on 2-X-5-iodopyridine and 2-X-5-bromopyridine (X = F, Cl, Br and I) are characterized by using single-crystal X-ray diffraction analysis to examine the nature of C2−X2···A–Cu and C5−X5···A–Cu halogen bonds. The reaction of the 2,5-dihalopyridines and Cu(I) salts allows the synthesis of eight 1-D coordination polymers and a discrete structure. The resulting Cu(I)-complexes are linked by C−X···A–Cu halogen bonds forming 3-D supramolecular networks. The C−X···A–Cu halogen bonds formed between halopyridine ligands and copper(I)-bound halide ions are stronger than C−X···X’–C interactions between two 2,5-dihalopyridine ligands. The C5−I5···I–Cu and C5−Br5···Br–Cu halogens bonds are shorter for C2-fluorine than C2-chlorine due to the greater electron-withdrawing power of fluorine. In 2,5-diiodopyridine-Cu(I)Br complex, the shorter C2−I2···Br–Cu [3.473(5) Å] distances are due to the combined polarization of C2-iodine by C2−I2···Cu interactions and para-electronic effects offered by the C5-iodine, whilst the long halogen bond contacts for C5−I5···Br–Cu [3.537(5) Å] are indicative that C2-iodine has a less para-electronic influence on the C5-iodine. In 2-fluoro-5-X-pyridine-Cu(I) complexes, the C2-fluorine is halogen bond passive, while the other C2-halogens in 2,5-dihalopyridine-Cu(I), including C2-chlorine, participate in halogen bonding interactions.

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49

Jiao, Min, Xiang Li, Jing Yu Liu, Yong Qiang Tian, Yu Huang, Chun Mei Gao, and Xin Jun Chen. "Study of Absorption of Heavy Metals (Pb,Cu) in Phragmites australis in Lingang New City." Applied Mechanics and Materials 692 (November 2014): 3–7. http://dx.doi.org/10.4028/www.scientific.net/amm.692.3.

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Analysis on the concentrations of Pb, Cu in the roots, stems, leaves of phragmites australis which grows on Lingang New City of Shanghai showed that both of Pb, Cu in roots were higher concentrations than that in stems and leaves; the absorption of Pb,Cu had obvious seasonal variation; in winter, the enrichment of Pb, Cu in phranmites autralis was occurred and the enrichment ability of Pb was higher than Cu,

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50

KWIATKOWSKI, M., E. KWIATKOWSKI, A. OLECHNOWICZ, G. BANDOLI, and A. DOLMELLA. "ChemInform Abstract: Copper(II) Complexes with the Tetraaza Ligands Resulting from Single Condensation Between Linear Triamines and Aromatic Aldehydes. Crystal Structure of (Cu(pyaDPT)I)I×MeOH, (Cu(pyaMeDPT)I)I×MeOH and (Cu(iqaMeDPT)I)I." ChemInform 24, no. 8 (August 20, 2010): no. http://dx.doi.org/10.1002/chin.199308205.

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