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1

S. Al-Janabi, Ahmed, Adnan A. Al-Dulaimi, Hayfa M. Gergees, and Mohammed H. Saleh. "Synthesis and Spectroscopic Studies of New Palladium(II) Complexes of N-hydroxymethyl Saccharin (Sac-CH2OH) and Amines or Diaminas Ligands." Oriental Journal of Chemistry 35, no. 1 (2019): 186–92. http://dx.doi.org/10.13005/ojc/350121.

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Treatment of the chelated palladium(II) complex, trans-[Pd(K2-Sac-CH2O)2].2H2O with one mole equivalent of the diammines (L-L), L-L = 2,2'-bipyridine (bipy),. ethylene diamine (en), 1,10-phenanthroline (phen), or N,N-dimethyl ethylene diammine (dmen) in EtOH solvent afforded mixed ligand complexes of the type [Pd(K1-Sac-CH2O)2(L-L)] in 82-93% yield. While treatment of trans-[Pd(K2-Sac-CH2O)2].2H2O with two mole equivalents of the monoamines (L), L=pyridine (py), 3-methylpyridine (3-mpy) or 3-aminopyridine (3-apy) in EtOH solvent gave trans-[Pd(K1-Sac-CH2O)2(L)2] complexes in 86-89% yield The p
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2

McCarthy, Sharon L., Robert J. Hinde, Kenneth J. Miller, Janet S. Anderson, Harold Basch, and Morris Krauss. "The binding of substitutedcis-Pt(II)-diammines to duplex DNA." Biopolymers 29, no. 4-5 (1990): 785–90. http://dx.doi.org/10.1002/bip.360290412.

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3

Il’in, M. A., V. A. Emel’yanov, and I. A. Baidina. "Structure and synthesis of nitrosoruthenium trans-diammines [Ru(NO)(NH3)2Cl3] and [Ru(NO)(NH3)2(H2O)Cl2]Cl·H2O." Journal of Structural Chemistry 49, no. 6 (2008): 1090–97. http://dx.doi.org/10.1007/s10947-008-0183-4.

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4

Tsoi, J., and Sai Ying Pun. "Diamine or diammine." British Dental Journal 229, no. 2 (2020): 73. http://dx.doi.org/10.1038/s41415-020-1942-7.

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5

Rochon, Fernande D., Robert Melanson, Jean-Pierre Macquet, Francine Belanger-Gariepy, and Andre L. Beauchamp. "Crystal structures of diammine(oxalato)platinum(II)and diammine(malonato)platinum(II)." Inorganica Chimica Acta 108, no. 1 (1985): 1–6. http://dx.doi.org/10.1016/s0020-1693(00)84314-5.

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6

Chen, Catherine K. J., Peter Kappen, Dan Gibson, and Trevor W. Hambley. "trans-Platinum(iv) pro-drugs that exhibit unusual resistance to reduction by endogenous reductants and blood serum but are rapidly activated inside cells: 1H NMR and XANES spectroscopy study." Dalton Transactions 49, no. 23 (2020): 7722–36. http://dx.doi.org/10.1039/d0dt01622e.

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7

Bréhin, P., J. C. Chottard, J. Kozelka, and C. Bois. "Diammine(dimethylmalonato)platinum(II) Monohydrate." Acta Crystallographica Section C Crystal Structure Communications 52, no. 5 (1996): 1186–88. http://dx.doi.org/10.1107/s010827019501482x.

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8

Kraus, Florian, Matthias B. Fichtl, and Sebastian A. Baer. "Beryllium Diammine Difluoride [BeF2(NH3)2]." Zeitschrift für Naturforschung B 64, no. 3 (2009): 257–62. http://dx.doi.org/10.1515/znb-2009-0301.

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Beryllium difluoride BeF2 reacts with liquid ammonia forming discrete diammine difluoro beryllium( II) [BeF2(NH3)2] molecules. The colorless compound crystallizes in the monoclinic space group P21/c with a = 4.8815(2), b = 6.8528(3), c = 10.3690(5) Å, β = 92.01(1)◦, V = 346.65(3) Å3 at 123 K with Z = 4. [BeF2(NH3)2] is the first structurally characterized example of a berylliumammonia complex. The compound has been investigated further by Raman, IR, and DTA-TG measurements and by quantum chemical ELF, AIM and NBO calculations.
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9

Xiang, Jing, Ye-Gao Yin, and Xiao-Chun Huang. "Diammine(pyridine-2,6-dicarboxylato)copper(II)." Acta Crystallographica Section E Structure Reports Online 62, no. 1 (2005): m4—m6. http://dx.doi.org/10.1107/s1600536805037256.

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10

Olszewski, Ulrike, Florian Ach, Ernst Ulsperger, et al. "In Vitro Evaluation of Oxoplatin: An Oral Platinum(IV) Anticancer Agent." Metal-Based Drugs 2009 (June 30, 2009): 1–11. http://dx.doi.org/10.1155/2009/348916.

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Platinum(IV) compounds like oxoplatin (cis, cis, trans-diammine-dichlorido-dihydroxido-platinum(IV)) show increased stability and therefore can be applied orally. In a panel of 38 human cancer cell lines this drug induced S-phase arrest and cell death with IC50 values 2.5-fold higher than cisplatin. Oxoplatin may be converted to cisplatin by intracellular reducing agents, however, exposure to 0.1 M HCl mimicking gastric acid yielded cis-diammine-tetrachlorido-platinum(IV) exhibiting twofold increased activity. Similar results were obtained for another platinum(IV) compound, JM 149 (ammine-dich
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11

Li, R., E. C. M. Lo, B. Y. Liu, M. C. M. Wong, and C. H. Chu. "Randomized Clinical Trial on Preventing Root Caries among Community-Dwelling Elders." JDR Clinical & Translational Research 2, no. 1 (2016): 66–72. http://dx.doi.org/10.1177/2380084416668491.

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Dental root caries is a common disease among elders. More efforts on preventing this disease are needed. Silver diammine fluoride (SDF) is known to prevent dental caries in primary teeth. However, clinical evidence of its efficacy in preventing root surface caries is limited. This clinical trial aimed to compare the effectiveness of SDF in preventing root caries among elders in a water fluoridated area. A total of 323 elders who had at least 5 teeth with exposed root surfaces and who had self-care ability were randomly allocated into 3 intervention groups: group 1 (placebo control), annual app
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12

Wang, Qing-Kun, Shao-Ping Pu, Yan-Wei Cong, Yong-Nian Li та Chun-Fang Luan. "cis-Diammine(glycolato-κ2O1,O2)platinum(II)". Acta Crystallographica Section E Structure Reports Online 65, № 12 (2009): m1687. http://dx.doi.org/10.1107/s1600536809049757.

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13

Ye, Q. S., M. J. Xie, W. P. Liu, et al. "Crystal structure of diammine(malonato)palladium(II)." Journal of Structural Chemistry 52, no. 1 (2011): 212–15. http://dx.doi.org/10.1134/s0022476611010318.

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14

Watanabe, T., M. Takano, A. Ogasawara, et al. "Anti-Candida Activity of a New Platinum Derivative." Antimicrobial Agents and Chemotherapy 44, no. 10 (2000): 2853–54. http://dx.doi.org/10.1128/aac.44.10.2853-2854.2000.

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ABSTRACT A new platinum derivative of the form H[Pt(IV)(Hdigly)Cl2(OH)2] (Hdiglyglycylglycine) damaged the Candida albicans cell membrane and inhibited the growth of the cells. The cytotoxic activity of H[Pt(IV)(Hdigly)Cl2(OH)2] on mammalian cells was 10-fold lower than that ofcis-diammine-dichloroplatinum (cisplatin). Substitution of platinum for peptides is effective for enhancement of antifungal activity and reduction of the toxicity to mammalian cells.
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15

Gökaugaç, G., L. Tatar, D. Kisakürek, and D. Ülkü. "Diamminebis(2,4,6-trichlorophenolato)copper(II)." Acta Crystallographica Section C Crystal Structure Communications 55, no. 9 (1999): 1413–16. http://dx.doi.org/10.1107/s0108270199006447.

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16

Viossat, B., P. Khodadad, and N. Rodier. "Structure du diammine(oxo-5 prolinato)platine(II)." Acta Crystallographica Section C Crystal Structure Communications 47, no. 8 (1991): 1714–16. http://dx.doi.org/10.1107/s0108270191001063.

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17

Brown, C. J., D. S. Cook, and L. Sengier. "Diamminebis[N'-(2-pyrimidinyl)sulfanilamido]copper." Acta Crystallographica Section C Crystal Structure Communications 43, no. 12 (1987): 2332–34. http://dx.doi.org/10.1107/s0108270187087869.

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18

Díaz, Jesús García, Atzimba García Albor, Espino Valencia Jaime, Viktor Vrábel та Jozef Kožíšek. "Poly[diamminedi-μ3-dicyanamido-copper(II)]". Acta Crystallographica Section E Structure Reports Online 68, № 12 (2012): i89—i90. http://dx.doi.org/10.1107/s1600536812045382.

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19

Roszak, A. W., P. Milne, and D. F. Weaver. "Diamminebis(5,5-diphenylhydantoinato)zinc(II) Hemihydrate." Acta Crystallographica Section C Crystal Structure Communications 51, no. 7 (1995): 1297–300. http://dx.doi.org/10.1107/s0108270195000291.

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20

Tatar, Leyla, Gülsün Gökağac, and Dinçer Ülkü. "Diamminebis(2,4,6-tribromophenolato-O)copper(II)." Acta Crystallographica Section C Crystal Structure Communications 56, no. 6 (2000): 668–69. http://dx.doi.org/10.1107/s0108270100003966.

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21

Kimura, Shigezo, Yosuke Nakajima, Shintaro Hasegawa, and Hiroshi Tazaki. "STUDY ON NEPHROTOXICITY IN RATS RECEIVING CIS-DIAMMINE-1, 1-CYCLOBUTANEDICARBOXYLATE PLATINUM II." Japanese Journal of Urology 80, no. 4 (1989): 517–25. http://dx.doi.org/10.5980/jpnjurol1989.80.517.

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22

Utsuno, Shunji, Yuzo Yoshikawa, and Yoshimi Tahata. "Stereochemical studies of the diammine(triethylenetetramine)cobalt(III) complex." Inorganic Chemistry 24, no. 18 (1985): 2724–26. http://dx.doi.org/10.1021/ic00212a004.

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23

Xiang, Jing, та Xiang-Cheng Lin. "Diammine[pyridine-2,6-dicarboxylato-κ3O2,N,O6]zinc(II)". Acta Crystallographica Section E Structure Reports Online 62, № 3 (2006): m593—m594. http://dx.doi.org/10.1107/s1600536806004557.

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24

Mackay, Fiona S., Julie A. Woods, Harry Moseley, et al. "A Photoactivatedtrans-Diammine Platinum Complex as Cytotoxic as Cisplatin." Chemistry - A European Journal 12, no. 11 (2006): 3155–61. http://dx.doi.org/10.1002/chem.200501601.

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25

Woidy, Patrick, and Florian Kraus. "The Diammine Silver(I) Acetate [Ag(NH3)2]OAc." Zeitschrift für anorganische und allgemeine Chemie 639, no. 14 (2013): 2643–47. http://dx.doi.org/10.1002/zaac.201300338.

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26

Kraus, Florian, Matthias Fichtl, and Sebastian Baer. "Crystal structure of [Ag(NH3)3]2[Ag(NH3)2]2[SnF6]F2, a compound showing argentophilic interactions." Acta Crystallographica Section E Crystallographic Communications 72, no. 12 (2016): 1860–63. http://dx.doi.org/10.1107/s2056989016019010.

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Bis[triamminesilver(I)] bis[diamminesilver(I)] hexafluoridostannate(IV) difluoride, [Ag(NH3)3]2[Ag(NH3)2]2[SnF6]F2, was obtained in the form of colourless crystals from the reaction of CsAgSnF7in anhydrous ammonia. Two different ammine complexes of silver(I) are present in the structure,i.e.a linear diammine and a T-shaped triammine complex. The ammine silver(I) complexes show Ag...Ag distances in the range of argentophilic interactions. In the crystal, several N—H...F hydrogen bonds are present between the complex cations and the SbF6−and F−anions, leading to the formation of a three-dimensio
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27

Benson, Ronda L., Koichi Iwata, William L. Weaver, and Terry L. Gustafson. "Improvements in the Generation of Quasi-Continuous, Tunable Ultraviolet Excitation for Raman Spectroscopy: Applications to Drug/Nucleotide Interactions." Applied Spectroscopy 46, no. 2 (1992): 240–45. http://dx.doi.org/10.1366/0003702924125591.

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We demonstrate the generation of quasi-continuous ultraviolet excitation at wavelengths shorter than 240 nm using the frequency-doubled output of a synchronously pumped picosecond dye laser operating in the region of 420 nm. Owing to the relatively low peak power but high average power of the system, we obtain high-quality resonance Raman spectra at wavelengths as short as 209 nm. We apply the source to the study of the binding of anticancer drugs to DNA. In particular, we compare the binding of cis-diamminedichloroplatinum (II) (cisplatin) and cis-diammine-1, 1-cyclobutane dicarboxylate plati
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28

Briz, Oscar, Maria Angeles Serrano, Noemi Rebollo, et al. "Carriers Involved in Targeting the Cytostatic Bile Acid-Cisplatin Derivativescis-Diammine-chloro-cholylglycinate-platinum(II) andcis-Diammine-bisursodeoxycholate-platinum(II) toward Liver Cells." Molecular Pharmacology 61, no. 4 (2002): 853–60. http://dx.doi.org/10.1124/mol.61.4.853.

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29

De Pascali, Sandra Angelica, Antonella Muscella, Santo Marsigliante, Maria Grazia Bottone, Graziella Bernocchi, and Francesco Paolo Fanizzi. "Cisplatin-related drugs for nongenomic targets: Forcing the reactivity with nucleobases." Pure and Applied Chemistry 85, no. 2 (2012): 355–64. http://dx.doi.org/10.1351/pac-con-12-08-07.

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The products obtained by forcing the reaction with nucleosides (guanosine, Guo, and adenosine, Ado) of potential anticancer drugs for nongenomic targets [PtCl(O,O'-acac)(L)] (L = dimethyl sulfoxide, DMSO; dimethyl sulfide, DMS), closely related to their very powerful organometallic analogues [Pt(O,O'-acac)(γ-acac)(L)], have been studied. [PtCl(O,O'-acac)(L)] and [Pt(O,O'-acac)(γ-acac)(L)] complexes were reported unreactive toward nucleobases. Aquo species [Pt(O,O'-acac)H2O(L)]+, obtained from [PtCl(O,O'-acac)(L)] by Ag+ driven coordinated Cl– removal, gave access to [Pt(O,O'-acac)(L)(nucleosid
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30

Rudolphus, A., R. Heinzel-Wieland, V. A. M. M. Vincent, et al. "Oxidation-resistant variants of recombinant anti-leucoprotease are better inhibitors of human-neutrophil-elastase-induced emphysema in hamsters than natural recombinant antileucoprotease." Clinical Science 81, no. 6 (1991): 777–84. http://dx.doi.org/10.1042/cs0810777.

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1. Antileucoprotease, being sensitive to oxidative inactivation, can be produced by recombinant techniques. Via site-directed mutagenesis, two mutants of recombinant antileucoprotease were produced in which one or more of the oxidation-sensitive methionine residues were replaced by leucine: in rALP242, methionine-73 was replaced by leucine, and in rALP231, leucine was substituted for four methionine residues. In vitro, native antileucoprotease and the recombinant antileucoprotease preparations have similar inhibitory characteristics towards human neutrophil elastase. We hypothesized that repla
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31

ORTEGA, RICHARD. "APPLICATIONS OF NUCLEAR MICROPROBE ANALYSIS IN CANCER CELL BIOLOGY AND PHARMACOLOGY." International Journal of PIXE 09, no. 03n04 (1999): 235–44. http://dx.doi.org/10.1142/s0129083599000334.

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Nuclear microprobe analysis studies in cancer cell pharmacology and biology carried out at Bordeaux-Gradignan are reported. The cellular pharmacology of two anticancer agents, cis-diammine-dichloroplatinum(II), and 4′-iodo-4′-deoxy-doxorubicin, were investigated, as well as the role of iron in neuroblastoma carcinogenesis, and chromium(III) in trans-generation carcinogenesis. Nuclear microprobe analysis, using PIXE and particle backscattering microanalysis, was able to reveal intracellular and tissue distributions of the elements under investigation. Moreover, the fully quantitative and multi-
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32

Tanabe, Noboru, Mitsuyoshi Goto, Hiroyuki Morita, et al. "Pharmacokinetics of Cis-Diammine-Dichlor-Platin in a Hemodialysis Patient." Cancer Investigation 9, no. 6 (1991): 629–35. http://dx.doi.org/10.3109/07357909109039874.

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33

Dentzer, J., P. Ehrburger, and J. Lahaye. "Adsorption and decomposition of silver diammine complexes on carbon surfaces." Journal of Colloid and Interface Science 112, no. 1 (1986): 170–77. http://dx.doi.org/10.1016/0021-9797(86)90079-2.

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34

KO, Aye KO, Naoko MATSUI, Ayako NAKAMOTO, et al. "Effect of silver diammine fluoride application on dentin bonding performance." Dental Materials Journal 39, no. 3 (2020): 407–14. http://dx.doi.org/10.4012/dmj.2019-057.

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35

McCarthy, Sharon L., Robert J. Hinde, Kenneth J. Miller, Janet S. Anderson, Harold Basch, and Morris Krauss. "Theoretical studies ofcis-Pt(II)-diammine binding to duplex DNA." Biopolymers 29, no. 4-5 (1990): 823–36. http://dx.doi.org/10.1002/bip.360290416.

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36

Brehin, P., J. Kozelka, J. P. Girault, C. Bois, and J. C. Chottard. "Thermodynamic and kinetic stabilities of substituted-malonato platinum diammine complexes." Journal of Inorganic Biochemistry 43, no. 2-3 (1991): 600. http://dx.doi.org/10.1016/0162-0134(91)84571-p.

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37

Gökaǧaç, Gülsün, Muammer Sonsuz, Fatih Şen, and Duygu Kısakürek. "Atom Transfer Rearrangement Radical Polymerization of Diamminebis( 2,4,6-trihalophenolato)copper(II) Complexes in the Solid State." Zeitschrift für Naturforschung B 61, no. 10 (2006): 1222–28. http://dx.doi.org/10.1515/znb-2006-1006.

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The synthesis of the poly(dichloro- or dibromophenylene oxide)s was achieved by the thermal decomposition of diammine-bis(2,4,6-trihalophenolato)copper(II) complexes in the solid state by atom transfer rearrangement radical polymerization. The thermal decomposition was performed either at different temperature ranges, 110 - 250 °C, for 3 h, or at the maximum conversion temperature for different time intervals, 3 - 48 h. Maximum yields of polymers were obtained at 190 °C and 3 h. The polymers were characterized by FTIR, 1H and 13C NMR spectroscopy, SEM, TGA and molecular weight determination by
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38

SAYED, Mahmoud, Toru NIKAIDO, Ahmed ABDOU, Michael F. BURROW, and Junji TAGAMI. "Potential use of silver diammine fluoride in detection of carious dentin." Dental Materials Journal 40, no. 3 (2021): 820–26. http://dx.doi.org/10.4012/dmj.2020-308.

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39

Castillo, J. L., S. Rivera, T. Aparicio, et al. "The Short-term Effects of Diammine Silver Fluoride on Tooth Sensitivity." Journal of Dental Research 90, no. 2 (2010): 203–8. http://dx.doi.org/10.1177/0022034510388516.

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40

Mironov, I. V. "Stability of diammine and chloroammine gold(I) complexes in aqueous solution." Russian Journal of Inorganic Chemistry 52, no. 6 (2007): 960–62. http://dx.doi.org/10.1134/s003602360706023x.

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41

Khodadad, P., and N. Rodier. "trans-Diammine-trans-dichloro-trans-dihydroxoplatine(IV) di(peroxyde d`hydrogène)." Acta Crystallographica Section C Crystal Structure Communications 43, no. 11 (1987): 2219–20. http://dx.doi.org/10.1107/s0108270187088383.

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42

Aschwanden, S., H. W. Schmalle, A. Reller, and H. R. Oswald. "Preparation, crystal structure, thermal and catalytical behaviour of copper diammine divanadate." Materials Research Bulletin 28, no. 1 (1993): 45–58. http://dx.doi.org/10.1016/0025-5408(93)90007-z.

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43

Matsumoto, K., K. Takahashi, and T. Watanabe. "Synthesis and chemical properties of cis-diammine-platinum 3,3-dimethylglutarimide blue." Inorganica Chimica Acta 121, no. 2 (1986): L29—L31. http://dx.doi.org/10.1016/s0020-1693(00)84502-8.

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44

Engel, W. "Thermoanalytical Investigation of Stored Ammonium Nitrate doped with diammine copper-(II)." Propellants, Explosives, Pyrotechnics 10, no. 3 (1985): 84–86. http://dx.doi.org/10.1002/prep.19850100308.

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45

Ferraro, A., M. Eufemi, L. Cervoni, F. Altieri, and C. Turano. "DNA-nuclear matrix interactions analyzed by cross-linking reactions in intact nuclei from avian liver." Acta Biochimica Polonica 42, no. 2 (1995): 145–51. http://dx.doi.org/10.18388/abp.1995_4638.

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To detect the interactions of DNA with the nuclear matrix proteins, DNA-protein cross-linkages were induced in intact nuclei from chicken liver by the use of cis-diammine dichloroplatinum. Methods have been devised for fast purification both of the proteins and of the DNA fragments involved in the cross-linked complexes. By Southern-Western blotting a number of matrix proteins isolated from the complexes have been shown to recognize specifically DNA sequences present in the cross-linked DNA fragments. This experimental approach not only allows to identify the nuclear matrix-DNA interactions ex
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46

Kahlenberg, Volker, Thomas Gelbrich, Richard Tessadri та Frederik Klauser. "Crystal structure ofcis-diamminebis(nitrito-κN)platinum(II)". Acta Crystallographica Section E Crystallographic Communications 71, № 4 (2015): 366–70. http://dx.doi.org/10.1107/s2056989015004879.

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Single crystals ofcis-[Pt(NO2)2(NH3)2], were obtained by means of hypersaturation directly out of a plating electrolyte. The square-planar coordination environment of the divalent PtIIatom is formed by four N atoms belonging to two ammine and two monodentate nitrite ligands. The ligands adopt acisconfiguration. The crystal structure contains stacks of close-packed molecules which run parallel to [001]. There are nine crystallographically independent intermolecular N—H...O hydrogen bonds, resulting in a hydrogen-bondedhxl-type framework in which each molecule serves as an eight-connected node.
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47

Brown, B. E., and C. J. L. Lock. "trans-Diamminebis(1-methylcytosine-N3)platinum(II) diperchlorate." Acta Crystallographica Section C Crystal Structure Communications 44, no. 4 (1988): 611–14. http://dx.doi.org/10.1107/s0108270187011764.

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48

Johnson, D. A., D. Y. Jeter, and A. W. Cordes. "Structure of sodium diamminebis(hydrogensulfito)disulfitoruthenate(II) hexahydrate." Acta Crystallographica Section C Crystal Structure Communications 43, no. 10 (1987): 2001–2. http://dx.doi.org/10.1107/s0108270187089297.

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Xu, L., D. Xu, Y. Xu, and J. Gu. "Diamminebis[dimethylglyoximato(1–)]cobalt(III) Fluoborate and Perchlorate." Acta Crystallographica Section C Crystal Structure Communications 52, no. 5 (1996): 1119–22. http://dx.doi.org/10.1107/s010827019501568x.

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50

Dołęga, Anna, Sylwia Godlewska, and Katarzyna Baranowska. "Diamminebis(tri-tert-butoxysilanethiolato)cadmium(II) acetonitrile solvate." Acta Crystallographica Section E Structure Reports Online 62, no. 12 (2006): m3567—m3569. http://dx.doi.org/10.1107/s1600536806049695.

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