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Journal articles on the topic 'Glycinato'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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1

Higuchi, Takeshi, Ayana Uchida та Masato Hashimoto. "Calcium and strontium salts of (glycinato-κ2N,O)oxidobis(peroxido-κ2O,O′)vanadate(V) tetrahydrate". Acta Crystallographica Section C Crystal Structure Communications 69, № 12 (2013): 1494–97. http://dx.doi.org/10.1107/s0108270113031181.

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The title salts calcium (glycinato-κ2N,O)oxidobis(peroxido-κ2O,O′)vanadate(V) tetrahydrate, Ca[VO(O2)2(NH2CH2COO)]·4H2O, and strontium (glycinato-κ2N,O)oxidobis(peroxido-κ2O,O′)vanadate(V) tetrahydrate, Sr[VO(O2)2(NH2CH2COO)]·4H2O, crystallized at pHca7.4 with similar lattice parameters. The glycinate anion acts as a bidentateN,O-chelating ligand, and the V atom has a pentagonal bipyramidal geometry, with two η2-peroxo groups and the glycinate N atom in the equatorial plane, and one terminal oxo and a glycinate O atom at the axial positions. The H atoms of three of the four water molecules in

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2

Kim, Jung-Sung, Woo-Sik Jung, Hiroshi Tomiyasu, and Hiroshi Fukutomi. "Kinetics and Mechanism of Replacement of Glycinate in Bis(glycinato)oxovanadium(IV) by Oxalate." Bulletin of the Chemical Society of Japan 59, no. 2 (1986): 613–16. http://dx.doi.org/10.1246/bcsj.59.613.

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3

Dewan, J. C. "Structure of tris(glycinato)cobalt(III) dihydrate." Acta Crystallographica Section C Crystal Structure Communications 44, no. 12 (1988): 2199–201. http://dx.doi.org/10.1107/s0108270188009126.

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4

Morris, David M., and Joseph S. Merola. "Octametallic Cluster of Cp*Ir(glycinato) Cations." ACS Omega 4, no. 26 (2019): 22126–32. http://dx.doi.org/10.1021/acsomega.9b03267.

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5

Klausmeyer, Kevin K., Rafael A. Adrian та Marsha M. Yaklin. "Tetraethylammonium acetonitriletricarbonyl(glycinato-κ2N,O)molybdenum(0)". Acta Crystallographica Section E Structure Reports Online 62, № 12 (2006): m3368—m3369. http://dx.doi.org/10.1107/s1600536806047684.

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6

Gu, Ke-Qiang, Yu-Xi Sun, Ran Zhang, Nian-Wei Zhang та Hong-Wen Che. "Tris(glycinato-κ2 N,O)cobalt(III)". Acta Crystallographica Section E Structure Reports Online 63, № 3 (2007): m740—m742. http://dx.doi.org/10.1107/s1600536807005636.

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The title compound, [Co(C2H4NO2)3], is a mononuclear cobalt(III) complex. The CoIII atom is six-coordinated by three N atoms and three O atoms from three chelating glycinate ligands, forming a slightly distorted octahedral configuration. In the crystal structure, the molecules are linked together by intermolecular N—H...O hydrogen bonds, forming a three-dimensional network.

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7

Islam, M. N., S. M. S. Shahriar, M. K. Islam, M. Jesmin, M. M. Ali, and J. A. Khanam. "Antibacterial Activities of Some Transition Metal Schiff Base Complexes." International Letters of Chemistry, Physics and Astronomy 10 (September 2013): 12–20. http://dx.doi.org/10.18052/www.scipress.com/ilcpa.10.12.

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A new series of four transition metal complexes of a Schiff base derived from salicylaldehyde and glycine, viz. [N-salicylidene glycinato diaqua cobalt (II) dimer] (SGCo)2, [N-salicylideneglycinato-di-aqua-nickel(ll)dimer] (SGN)2, [N-salicylideneglycinato-aqua-copper(II)] (SGC) and [N-salicylidene glycinato diaqua zinc(II) dimer] (SGZ)2 have been synthesized and characterized through a rapid, simple, and efficient methodology in excellent yield. These compounds were screened for In Vitro antibacterial activities against six pathogenic bacteria, such as Shigella sonnei, Escherichia coli, Bacilu

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8

Islam, M. N., S. M. S. Shahriar, M. K. Islam, M. Jesmin, M. M. Ali, and J. A. Khanam. "Antibacterial Activities of Some Transition Metal Schiff Base Complexes." International Letters of Chemistry, Physics and Astronomy 10 (March 18, 2013): 12–20. http://dx.doi.org/10.56431/p-ctv1g0.

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A new series of four transition metal complexes of a Schiff base derived from salicylaldehyde and glycine, viz. [N-salicylidene glycinato diaqua cobalt (II) dimer] (SGCo)2, [N-salicylideneglycinato-di-aqua-nickel(ll)dimer] (SGN)2, [N-salicylideneglycinato-aqua-copper(II)] (SGC) and [N-salicylidene glycinato diaqua zinc(II) dimer] (SGZ)2 have been synthesized and characterized through a rapid, simple, and efficient methodology in excellent yield. These compounds were screened for In Vitro antibacterial activities against six pathogenic bacteria, such as Shigella sonnei, Escherichia coli, Bacilu

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9

NONGMAITHEM, RAJMUHON SINGH, RAJEN SINGH NONGMAITHEM, and MANIHAR SINGH AKOIJAM. "Studies on Outer-sphere Association of Tris( 1-amidino-O- alkylurea)- and Glycinato-bis( 1-amidino-O-methylurea)- cobalt(III) Complexes." Journal of Indian Chemical Society Vol. 73, Aug 1996 (1996): 419–21. https://doi.org/10.5281/zenodo.5897906.

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Department of Chemistry, Manipur University, Imphal-795 003 <em>Manuscript received 4 November 1993, revised 29 November 1994, accepted 29 December 1994</em> Studies on Outer-sphere Association of Tris( 1-amidino-<em>O</em>- alkylurea)- and Glycinato-bis( 1-amidino-<em>O</em>-methylurea)- cobalt(III) Complexes.

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10

Correia, Valdir R., Adailton J. Bortoluzzi, Ademir Neves, Antônio C. Joussef, Marcia G. M. Vieira, and Suzana C. Batista. "Bis[N-(2-pyridylmethyl)glycinato]zinc(II) dihydrate." Acta Crystallographica Section E Structure Reports Online 59, no. 7 (2003): m464—m466. http://dx.doi.org/10.1107/s1600536803012364.

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11

Reddy, G. Sudhakar, and Grant Gill Smith. "Ultrasound promoted N-benzylation of metal glycinato complexes." Inorganica Chimica Acta 133, no. 1 (1987): 1–2. http://dx.doi.org/10.1016/s0020-1693(00)84356-x.

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12

Petrür, František, and František Jursík. "Bis(glycinato)-kobalt(II), Darstellung und einige Eigenschaften." Zeitschrift für Chemie 8, no. 3 (2010): 116–17. http://dx.doi.org/10.1002/zfch.19680080322.

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13

Norman, R. E., N. J. Rose, and R. E. Stenkamp. "Mono-amino-acid–copper complexes: syntheses and structures of chloro(glycinato)(methanol)copper(II) and chloro(glycinato)(1-methylimidazole)copper(II)." Acta Crystallographica Section C Crystal Structure Communications 46, no. 1 (1990): 1–6. http://dx.doi.org/10.1107/s0108270189005238.

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14

Hodzic, I. M., and S. R. Niketic. "Synthesis and characterization of a novel (glycinato-N,O) yttrium(III) complex." Journal of the Serbian Chemical Society 66, no. 5 (2001): 331–34. http://dx.doi.org/10.2298/jsc0105331h.

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A novel yttrium(III) complex with glycine has been synthesized starting from tris(ethanedioato-O,O)yttrium(III) by the substitution of the acetylacetonato chelate ligands with glycine. The reaction product was purified by ion-exchange chromatography and characterized on the basis of infrared spectroscopy. The structure of the productwas tentatively established as tris(glycinato-N,O)yttrium(III) dihydrate.

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15

Gao, Sheng-Li, Yi-Zhi Li, Fei Ren, Qi-Zhen Shi та Liu-Fang Wang. "catena-Poly[[[diaqualanthanum(III)]-tri-μ-glycinato] trichloride monohydrate]". Acta Crystallographica Section E Structure Reports Online 58, № 5 (2002): m234—m236. http://dx.doi.org/10.1107/s1600536802007444.

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16

Revathi, Palanisamy, Thangavelu Balakrishnan, Kandasamy Ramamurthi та Subbiah Thamotharan. "Crystal structure ofcatena-poly[[[triaquastrontium]-di-μ2-glycinato] dibromide]". Acta Crystallographica Section E Crystallographic Communications 71, № 7 (2015): 875–78. http://dx.doi.org/10.1107/s2056989015012219.

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In the title coordination polymer, {[Sr(C2H5NO2)2(H2O)3]Br2}n, the Sr2+ion and one of the water molecules are located on twofold rotation axes. The alkaline earth ion is nine-coordinated by three water O atoms and six O atoms of the carboxylate groups of four glycine ligands, two in a chelating mode and two in a monodentate mode. The glycine molecule exists in a zwitterionic form and bridges the cations into chains parallel to [001]. The Br−counter-anions are located between the chains. Intermolecular hydrogen bonds are formed between the amino and carboxylate groups of neighbouring glycine li

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17

Alvarez-Larena, A., J. L. Briansó-Penalva, J. F. Piniella, R. Moreno-Esparza, L. Ruiz-Ramírez, and G. Ferrer-Sueta. "Aqua(glycinato)(3,4,7,8-tetramethyl-1,10-phenanthroline)copper(II) Nitrate." Acta Crystallographica Section C Crystal Structure Communications 51, no. 5 (1995): 852–54. http://dx.doi.org/10.1107/s0108270194013041.

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18

Zhao, Jiong-Peng, and Fu-Chen Liu. "Bis[N,N-bis(2-hydroxyethyl)glycinato]cobalt(II)." Acta Crystallographica Section E Structure Reports Online 66, no. 7 (2010): m848. http://dx.doi.org/10.1107/s1600536810023810.

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19

Casari, Barbara M., Amir H. Mahmoudkhani та Vratislav Langer. "A redetermination ofcis-aquabis(glycinato-κ2N,O)copper(II)". Acta Crystallographica Section E Structure Reports Online 60, № 12 (2004): m1949—m1951. http://dx.doi.org/10.1107/s1600536804030041.

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20

Khoo, Lian Ee, та Alan Hazell. "Polymeric [μ3-(N-phosphonomethyl)glycinato]tris(tri-n-butyltin)". Acta Crystallographica Section C Crystal Structure Communications 57, № 3 (2001): 254–56. http://dx.doi.org/10.1107/s0108270100018898.

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21

Wang, Jian-Ge, та Jian-Hua Qin. "catena-Poly[[[diaqualanthanum(III)]-tetrakis[μ-N-(4-acetamidophenylsulfonyl)glycinato]-[diaqualanthanum(III)]-bis[μ-N-(4-acetamidophenylsulfonyl)glycinato]] 4,4′-bipyridine disolvate tetradecahydrate]". Acta Crystallographica Section E Structure Reports Online 64, № 11 (2008): m1364—m1365. http://dx.doi.org/10.1107/s1600536808031450.

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22

Ozutsumi, Kazuhiko, and Hitoshi Ohtaki. "An X-Ray Diffraction Study on the Structures of Mono(glycinato)zinc(II) and Tris(glycinato)zincate(II) Complexes in Aqueous Solution." Bulletin of the Chemical Society of Japan 58, no. 6 (1985): 1651–57. http://dx.doi.org/10.1246/bcsj.58.1651.

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23

Yin, Li-Hui, Xu-Ping Liu, Lu-Yao Yi, Jin Wang, Ya-Jun Zhang, and Yu-Fei Feng. "Structural characterization of calcium glycinate, magnesium glycinate and zinc glycinate." Journal of Innovative Optical Health Sciences 10, no. 03 (2017): 1650052. http://dx.doi.org/10.1142/s1793545816500528.

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Metal glycinate chelates are formed by glycine and metal compounds through chemical reactions. Calcium glycinate, magnesium glycinate and zinc glycinate are kinds of new-type and ideal nutrient supplements, which have satisfactory physico-chemical properties and bioactivities. They are important for prophylaxis and treat metal deficiency. The structural characterization shows that the metal ion is bonded to the amino and carboxyl group to form two five-membered rings. This paper mainly studies the structure characterization of the metal chelated glycinates by their solubility, infrared spectru

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24

Wu, Lei, Guangxun Li, Migu He, Yingwei Wang, Gang Zhao, and Zhuo Tang. "First example of an organocatalytic asymmetric Mannich reaction between aldimines of glycinates and sulphonyl imines." Canadian Journal of Chemistry 94, no. 9 (2016): 769–72. http://dx.doi.org/10.1139/cjc-2016-0089.

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The catalytic enantioselective Mannich-type reaction between glycinate Schiff base and imines has been one of the most efficient routes for accessing α,β-diamino acids. However, the glycinate Schiff bases used in the references were almost ketimines. Only several examples of aldimines were used in the presence of metal catalyst. We developed the first example of an asymmetric direct Mannich reaction using aldimines of glycinates instead of ketimines of glycinates. The reaction was well catalyzed by chiral guanidine with high yield (up to 92%) and moderate stereoselectivity (up to 65%).

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25

Ambach, Eberhard, та Wolfgang Beck. "Metallkomplexe mit biologisch wichtigen Liganden XXVI : Reaktionen von Bis(α-aminoacidato)platin(II)-Komplexen mit Nitrosylsalzen: Nitrosylplatin-Komplexe[xxx] + X- (X = BF4 , PF6 , SbF6 )/Metal Complexes with Biologically Important Ligands XXXVI : Reaction of Bis(α-aminoacidato) Platinum(II) Complexes with Nitrosyl Salts: Nitrosyl Platinum Complexes[xxx]+X-(X = BF4 , PF6 , SbF 6)". Zeitschrift für Naturforschung B 40, № 2 (1985): 288–91. http://dx.doi.org/10.1515/znb-1985-0224.

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AbstractThe reactions of the glycinato, alaninato, or cyclo-leucinato chelate platinum complexes trans -[xxx] with nitrosyl salts NO+X- (X = BF4, PF6, SbF6) in acetonitrile at -20 °C give the blue nitrosyl compounds {(0N)Pt [xxx] X·nCH3CN. Nitrosation at the amino group is not observed. The spectroscopic data of the nitrosyl complexes (IR, XPE) are reported. [xxx] + PF6- reacts with lithium halides or halogens in DMF to give the platinum (IV) complexes X2Pt(NH2CH2CO2)2 (X = CI, Br, I).

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26

Bakir, Mohammed, Suzanne A. Clarke, Ishmael Hassan, Robert J. Lancashire та Marvadeen Singh-Wilmot. "trans-Bis(glycinato-κ2N,O)copper(II) 4-bromophenol solvate". Acta Crystallographica Section E Structure Reports Online 60, № 6 (2004): m868—m870. http://dx.doi.org/10.1107/s1600536804012541.

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27

Zou, Yang, Yin-Zhi Jiang, and Wei-Zu Wang. "Diaqua[N-(5-nitro-2-oxidobenzylidene)glycinato]copper(II) dihydrate." Acta Crystallographica Section E Structure Reports Online 66, no. 4 (2010): m455. http://dx.doi.org/10.1107/s1600536810010652.

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28

Moussa, S. M., R. R. Fenton, and Brendan J. Kennedy. "Studies of the Crystalline Forms of Bis(Glycinato)Copper(II)." Materials Science Forum 278-281 (April 1998): 912–17. http://dx.doi.org/10.4028/www.scientific.net/msf.278-281.912.

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29

Poznjak, Anatoli L., та Valerie I. Pavlovski. "Photodecarboxylierung von Mono-glycinato-bis π-akzeptorligand(lII)cobalt-Komplexen". Zeitschrift für Chemie 21, № 2 (2010): 74. http://dx.doi.org/10.1002/zfch.19810210213.

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30

Teo, Soon-Beng, Chew-Hee Ng, Siang-Guan Teoh, Hoong-Kun Fun, and Zhong-Yuan Zhou. "MANNICH REACTION OFBIS(GLYCINATO)COPPER(II), FORMALDEHYDE AND ACETAMIDE: X-RAY CRYSTAL STRUCTURE OF BIS[(N,N-DI-N'-METHYLACETAMIDO)GLYCINATO]COPPER(II) DIHYDRATE." Journal of Coordination Chemistry 35, no. 1-2 (1995): 35–40. http://dx.doi.org/10.1080/00958979508033083.

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31

SUVENDU, KUMAR MAZUMDAR, та MOHANTY PRAKASH. "Effect of Solvent on the Stability of some Novel Binuclear Complexes formed by trans-[(Co(en)2ClglyH]2+ and trans-[Co(en)2CIβ-alaH]2+ with few Transition Metal Ions". Journal of Indian Chemical Society Vol. 72, Jun 1995 (1995): 385–89. https://doi.org/10.5281/zenodo.5904963.

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Central Laboratory, Nalco, Angul Department of Chemistry, Utkal University, Vani Vihar, Bhubaneswar-751 004 <em>Manuscript received 14 May 1993, revised 26 November 1993, accepted 2 December 1993</em> The medium effect on the stability constant (log <em>K</em>) of [Co(en)<sub>2</sub>CiglyM]<sup>n+</sup> and [Co(en)<sub>2</sub>CIβ-ala]<sup>+</sup> (gly = glycinate, β-ala = β-alaninate, M(II) = Cu, Ni and Co) species has been investigated potentiometrically at 30° and <em>1</em> = 0.1 mol dm<sup>-3</sup>• The dielectric constant of the medium has been varied using methano

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32

Krishna, P. Murali, K. Hussain Reddy, N. Rashmitha, M. Sravanthi, and D. Sujathamma. "Synthesis and Characterization of Surfactant Assisted Copper Nanomaterials." Asian Journal of Chemistry 32, no. 11 (2020): 2700–2706. http://dx.doi.org/10.14233/ajchem.2020.22741.

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In this work, a simple and low cost synthetic method for four different copper nanomaterials having uniform shape and size using copper(II) acetate and cis-bis(glycinato)copper(II) complex in presence of non-ionic surfactants Tween-80 and Triton X-100 in the presence of ascorbic acid as reducing agent is described. The synthesized nanomaterials were characterized using FT-IR, UV-visible, powder XRD, EDX and SEM techniques. The characterization data reveals that all the copper nanomaterials formed are less than 30 nm size with spherical shape.

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33

Islam, Mohammad K., Md Nuruzzaman, Rashedul I. Ripon, et al. "Synthesis, Characterization and Bioactivities of Some Novel Oxovanadium(IV) Glycinato Complexes." European Scientific Journal, ESJ 14, no. 21 (2018): 410. http://dx.doi.org/10.19044/esj.2018.v14n21p410.

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The novel oxovanadium(IV) complexes, [VIVO(GlyH)(Gly)]+ClO4 - .H2O (1), [VIVO(GlyH)(Gly)]+NO3 - .H2O (2), [VIVO(GlyH)(Gly)]+CH3COO- .H2O (3) were synthesized and characterized by FT-IR, UV-Vis and 1H NMR spectroscopic measurements. The cumulative spectroscopic assessment envisaged that, the complexes adopt a square pyramidal structure, in which the two glycine ligands coordinate to vanadium(IV) center in bidentate fashions conforming a homoleptic structure. The amino nitrogen and a carboxylato oxygen atom coordinate the vanadium(IV) center from both sides making a five members chelate by each

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34

Tautermann, Christofer S., Jasmina Sabolović, Andreas F. Voegele, and Klaus R. Liedl. "Mechanism of the Cis−Trans Isomerization of Bis(glycinato)copper(II)." Journal of Physical Chemistry B 108, no. 6 (2004): 2098–102. http://dx.doi.org/10.1021/jp0364497.

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35

Handique, Jyotirekha G., and Jubaraj B. Baruah. "Oxidative oligomerisation of 2-naphthol by cis-bis(glycinato)copper(II)." Journal of Molecular Catalysis A: Chemical 166, no. 2 (2001): 225–31. http://dx.doi.org/10.1016/s1381-1169(00)00434-9.

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36

Kita, Ewa, Hasan Marai, Tadeusz Muzioł, and Karolina Lenart. "Kinetic studies on chromium-glycinato complexes in acidic and alkaline media." Transition Metal Chemistry 36, no. 1 (2010): 35–44. http://dx.doi.org/10.1007/s11243-010-9431-5.

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37

Ilan, Yigal, and Ariela Kfir. "Reactivity of cis-bis(glycinato ester)tetraammineruthenium(III) in acidic solutions." Inorganica Chimica Acta 156, no. 2 (1989): 221–26. http://dx.doi.org/10.1016/s0020-1693(00)83504-5.

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38

Gschwind, Fabienne, та Martin Jansen. "Poly[di-μ-glycinato-copper(II)]: a two-dimensional coordination polymer". Acta Crystallographica Section E Structure Reports Online 67, № 9 (2011): m1218—m1219. http://dx.doi.org/10.1107/s1600536811031503.

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39

Yoshimura, Yasuki. "Salt effect on the solubility of mer-(+)-tris(L-alaninato)cobalt(III)." Canadian Journal of Chemistry 76, no. 1 (1998): 71–77. http://dx.doi.org/10.1139/v97-200.

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The effect of NaF, NaCl, NaBr, NaI, NaNO3, CH3COONH4, NaH2PO4, and (NH4)2SO4 on mer-(+)-tris(L-alaninato)cobalt(III) (mer-(+)-[Co(L-ala)3]) was examined by determining the solubility of the chelate. While the solubility of mer-(+)-[Co(L-ala)3] (salting-in effect) increased with the addition of NaCl, NaBr, NaI, and NaNO3, the solubility (salting-out effect) decreased with the addition of NaF, CH3COONH4, and NaH2PO4. In low salt concentration (NH4)2SO4 caused slight salting-in, but in salt concentration >0.5 mol dm-3 (NH4)2SO4 brought about salting-out. The magnitude of the salting-in effect

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40

Yamaguchi, Hiromitsu, Yoshie Inomata, and Toshio Takeuchi. "Syntheses, properties, and crystal and molecular structures of bromo[N,N-bis(2-hydroxyethyl)glycinato]copper(II) and aquabromo[N,N-bis(2-hydroxyethyl)glycinato]copper(II)." Inorganica Chimica Acta 181, no. 1 (1991): 31–36. http://dx.doi.org/10.1016/s0020-1693(00)85256-1.

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41

Yodoshi, Masahiro, Mamiko Odoko та Nobuo Okabe. "Redetermination of (2,2′-bipyridyl-κ2N,N′)chloro(glycinato-κ2N:O)copper(II) dihydrate". Acta Crystallographica Section E Structure Reports Online 61, № 11 (2005): m2299—m2301. http://dx.doi.org/10.1107/s1600536805032265.

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42

Swaminathan, K., U. C. Sinha, C. Chatterjee, A. Phulambrikar, V. M. Padmanabhan, and R. Bohra. "Structure of [N,N-bis(carboxymethyl)glycinato](1,3-propanediamine)cobalt(III) monohydrate." Acta Crystallographica Section C Crystal Structure Communications 45, no. 4 (1989): 566–68. http://dx.doi.org/10.1107/s0108270188012995.

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43

Liu, Xu-Hui, Jin-Hua Cai, Yi-Min Jiang, Ying-Heng Huang та Xiu-Ju Yin. "Triaqua[N-(5-formysalicylidene)glycinato(2–)-κ3O,N,O′]nickel(II) monohydrate". Acta Crystallographica Section E Structure Reports Online 62, № 9 (2006): m2119—m2121. http://dx.doi.org/10.1107/s1600536806030698.

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44

Cai, Jin-Hua, Ying-Heng Huang та Yi-Min Jiang. "Triaqua[N-(5-formysalicylidene)glycinato(2–)-κ3O,N,O′]zinc(II) monohydrate". Acta Crystallographica Section E Structure Reports Online 62, № 10 (2006): m2432—m2434. http://dx.doi.org/10.1107/s1600536806034581.

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45

Xue, Ling-Wei, Xing-Wu Li, Gan-Qing Zhao та Qin-Long Peng. "catena-Poly[[pyridinecopper(II)]-μ-N-[(2-oxido-1-naphthyl)methylene]glycinato]". Acta Crystallographica Section E Structure Reports Online 65, № 10 (2009): m1237. http://dx.doi.org/10.1107/s1600536809037520.

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Li, Ya Min, Yong Hong Li та Cui Ping Zhai. "μ-Glycine-κ2O:O′-di-μ-sulfido-bis[(glycinato-κ2N,O)oxidomolybdenum(V)]". Acta Crystallographica Section E Structure Reports Online 63, № 12 (2007): m2931. http://dx.doi.org/10.1107/s1600536807054761.

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Hidalgo, M. A., J. Romero, J. Suárez-Varela, J. C. Avila-Rosón, and J. D. Martín-Ramos. "Diaqua[N-(2-ethylphenyl)-N-(carboxymethyl)glycinato-N,O,O'']copper(II)." Acta Crystallographica Section C Crystal Structure Communications 51, no. 8 (1995): 1512–14. http://dx.doi.org/10.1107/s0108270195002009.

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Kortes, Richard A., Fu-Tyan Lin, Rex E. Shepherd, and Chris Maricondi. "pH-dependent coordination of the glycinato donors of nitrilotriacetatoplatinate(II), [PtII(nta)]−." Inorganica Chimica Acta 245, no. 2 (1996): 149–56. http://dx.doi.org/10.1016/0020-1693(95)04822-7.

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Huang, Ying-Heng, Jin-Hua Cai, Xiu-Ju Yin та Yi-Min Jiang. "Triaqua[N-(5-formylsalicylidene)glycinato(2−)-κ3O,N,O′]cobalt(II) monohydrate". Acta Crystallographica Section E Structure Reports Online 62, № 11 (2006): m2922—m2924. http://dx.doi.org/10.1107/s1600536806041626.

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Yoshimura, Yasuki. "Anomalous Salting-Out Effect of Sodium Perchlorate onfac-Tris(glycinato)cobalt(III)." Bulletin of the Chemical Society of Japan 78, no. 4 (2005): 652–58. http://dx.doi.org/10.1246/bcsj.78.652.

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