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Journal articles on the topic 'Ambidentate'

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Published: 5 June 2025

Last updated: 1 August 2025

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1

Ghosh, Pokhraj, Manuel Quiroz, Randara Pulukkody, Nattamai Bhuvanesh, and Marcetta Y. Darensbourg. "Bridging cyanides from cyanoiron metalloligands to redox-active dinitrosyl iron units." Dalton Transactions 47, no. 34 (2018): 11812–19. http://dx.doi.org/10.1039/c8dt01761a.

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2

Valyaev, Dmitry A., Marina A. Uvarova, Alina A. Grineva, Vincent César, Sergei N. Nefedov, and Noël Lugan. "Post-coordination backbone functionalization of an imidazol-2-ylidene and its application to synthesize heteropolymetallic complexes incorporating the ambidentate IMesCO2−ligand." Dalton Transactions 45, no. 30 (2016): 11953–57. http://dx.doi.org/10.1039/c6dt02060g.

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The C4-carboxylation of the archetypal IMes ligand was achieved directly on its complexed form for the first time, and the resulting ambidentate IMes<sup>CO2−</sup>ligand was exploited for the formation of heteropolymetallic complexes.

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3

Melle, Philipp, Nathalie Ségaud, and Martin Albrecht. "Ambidentate bonding and electrochemical implications of pincer-type pyridylidene amide ligands in complexes of nickel, cobalt and zinc." Dalton Transactions 49, no. 36 (2020): 12662–73. http://dx.doi.org/10.1039/d0dt02482a.

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Pincer-type tridentate pyridyl bis(pyridylidene amide) (pyPYA<sub>2</sub>) ligand systems were coordinated to the Earth-abundant first row transition metals nickel, cobalt and zinc, revealing ambidentate N,N,N and O,N,O coordination behavior.

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4

Karsch, H. H. "Ambidentate, Anionic Phosphine Ligands in Organoelement Chemistry." Phosphorus, Sulfur, and Silicon and the Related Elements 77, no. 1-4 (1993): 41–44. http://dx.doi.org/10.1080/10426509308045614.

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5

Burmeister, J. "Ambidentate ligands, the schizophrenics of coordination chemistry." Coordination Chemistry Reviews 105, no. 1 (1990): 77–133. http://dx.doi.org/10.1016/0010-8545(90)80019-p.

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6

Graham, AJ, PC Healy, JD Kildea, and AH White. "Lewis-Base Adducts of Group 11 Metal(I) Compounds. XLVI. Synthesis and Conformational Systematics of Some Novel Polymeric Adducts of Pyridine-4-carbonitrile With Copper(I) Halides." Australian Journal of Chemistry 42, no. 1 (1989): 177. http://dx.doi.org/10.1071/ch9890177.

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The isolation and structural characterization of 1 : 1 adducts of copper(1) chloride (1) and bromide (2) with pyridine-4-carbonitrile (L) is described; crystals of the two complexes are isomorphous (monoclinic, P21/c, a ≈ 3.9, b ≈ 14.7, c ≈ 13.0 � , β ≈ 96°, Z 4; R0.047, 0.063 for No 630, 707 'observed' reflections respectively). Unlike the 1 : 1 adducts with the parent pyridine and benzonitrile ligands which are 'stair' polymers, these complexes comprise 'split-stair' strands woven into a two-dimensional sheet by crosslinking ambidentate ligands. Cu-N ( nitrile ) (1.942(9), 1.96(1) � ) are ap

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7

Kunze, Udo, Andreas Bruns, and Hussain Jawad. "Phosphinothioformamides - A Class of Versatile Ambidentate Complex Ligands." Phosphorous and Sulfur and the Related Elements 30, no. 1-2 (1987): 177–80. http://dx.doi.org/10.1080/03086648708080551.

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8

Abbasi, Alireza, Mikhail Yu Skripkin, Lars Eriksson, and Natallia Torapava. "Ambidentate coordination of dimethyl sulfoxide in rhodium(iii) complexes." Dalton Trans. 40, no. 5 (2011): 1111–18. http://dx.doi.org/10.1039/c0dt01026j.

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9

Vasil’chenko, I. S., T. E. Shestakova, V. N. Ikorskii, et al. "1-amino-2-thiobenzimidazoleimines as novel ambidentate ligand systems." Russian Journal of Coordination Chemistry 33, no. 3 (2007): 176–83. http://dx.doi.org/10.1134/s1070328407030049.

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10

Hsieh, Chung-Hung, Scott M. Brothers, Joseph H. Reibenspies, Michael B. Hall, Codrina V. Popescu, and Marcetta Y. Darensbourg. "Ambidentate Thiocyanate and Cyanate Ligands in Dinitrosyl Iron Complexes." Inorganic Chemistry 52, no. 4 (2013): 2119–24. http://dx.doi.org/10.1021/ic3025149.

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11

Matthews, Ray W., Mary McPartlin, and Ian J. Scowen. "Ambidentate binding in macrocyclic helicates: towards tuning secondary structure." Chemical Communications, no. 3 (1996): 309. http://dx.doi.org/10.1039/cc9960000309.

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12

BURMEISTER, J. L. "ChemInform Abstract: Ambidentate Ligands, the Schizophrenics of Coordination Chemistry." ChemInform 22, no. 8 (2010): no. http://dx.doi.org/10.1002/chin.199108362.

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13

KARSCH, H. H. "ChemInform Abstract: Ambidentate, Anionic Phosphine Ligands in Organoelement Chemistry." ChemInform 24, no. 36 (2010): no. http://dx.doi.org/10.1002/chin.199336215.

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14

López-Cardoso, Marcela, Patricia García y. García, Raymundo Cea-Olivares, and María Luisa Villareal. "Cytotoxic Activities of O-Cholesteryl-O-Phenyl-N-Phenylphosphoramidate and Its Organometallic Tin(lV) Derivatives." Metal-Based Drugs 8, no. 6 (2002): 333–35. http://dx.doi.org/10.1155/mbd.2002.333.

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O-Cholesteryl-O-phenyl-N-phenylphosphoramidate (1) and four organotin (lV) derivatives of the ambidentate O-cholesteryl-O -phenyl phosphorothioate ligand formulated as Me3 SnOSPR’R”(2), Ph3 SnOSPR’R”(3), O(CH2CH2S)2 Sn(n-Bu)OSPR’R”(4), S(CH2CH2S)2 Sn(n-Bu)OSPR’R”(5), (R’ = O-phenyl; R”= O-cholesteryl) were subjected to cytotoxicity screening against KB (nasopharingel carcinoma), OVCAR-5 (ovarium carcinoma) and SQC-1 UlSO (squamous cell cervix carcinoma) cell cultures. The results of the bioassay showed that these compounds possess potent antitumor activities against the studied human carcinoma

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15

Borodaev, S. V., M. E. Kletskii, and N. V. Shibaeva. "Ambidentate reactivity of 3-azapyrylium systems in nucleophilic attack reactions." Chemistry of Heterocyclic Compounds 30, no. 5 (1994): 612–15. http://dx.doi.org/10.1007/bf01169845.

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16

Spiro, Thomas G., and Alexandra V. Soldatova. "Ambidentate H-bonding of NO and O2 in heme proteins." Journal of Inorganic Biochemistry 115 (October 2012): 204–10. http://dx.doi.org/10.1016/j.jinorgbio.2012.05.013.

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17

Bíró, Linda, András Ozsváth, Réka Kapitány, and Péter Buglyó. "Pd(II) Binding Strength of a Novel Ambidentate Dipeptide-Hydroxypyridinonate Ligand; A Solution Equilibrium Study." Molecules 27, no. 14 (2022): 4667. http://dx.doi.org/10.3390/molecules27144667.

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A novel ambidentate dipeptide conjugate (H(L1)) containing N-donor atoms of the peptide part and an (O,O) chelate at the hydroxypyridinone (HP) ring is synthesized and characterized. It is hoped that this chelating ligand can be useful to obtain multitargeted Co(III)/Pt(II) dinuclear complexes with anticancer potential. The Pd(II) (as a Pt(II) model but with faster ligand exchange reactions) binding strength of the ligand was studied in an aqueous solution with the combined use of pH-potentiometry and NMR. In an equimolar solution, (L1)− was found to bind Pd(II) via the terminal amino and incr

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18

Vuckovic, Gordana, Zoran Miodragovic, and Sladjana Tanaskovic. "Preparation and properties of Cu(II) complexes with N,N’,N",N’’’-tetrakis(2-pyridylmethyl)-1,4,8,11-tetraazacyclotetradecane (tpmc) and pseudohalides(NCO- orNCSe-): Part II." Journal of the Serbian Chemical Society 69, no. 1 (2004): 17–23. http://dx.doi.org/10.2298/jsc0401017v.

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Two new Cu(II) complexes with N,N?,N",N???-tetrakis(2-pyridylmethyl) -1,4,8,11-tetraazacyclotetradecane (tpmc) and pseudohalides (NCO- or NCSe-) were isolated. Elemental analyses (C, H, N, Cu) corresponded to the formulas [Cu2(NCO)tpmc](ClO4)3. 2CH3CN and [Cu2(NCSe)2 tpmc] (ClO4)2. 2H2O. C2H5OH. The coordination mode of tpmc and these ambidentate pseudohalides, geometries spectral characteristics (VIS, IR) and other properties were compared with those of the previously described [Cu2(NCS)2tpmc] (ClO4)2. Antimicrobial activity towards selected bacteria and yeast was tested and found for the NCS

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19

Burlov, A. S., A. V. Tsukanov, G. S. Borodkin, et al. "Complexing properties of ambidentate benzo-15-crown-5-substituted azomethine ligands." Russian Journal of General Chemistry 76, no. 6 (2006): 992–96. http://dx.doi.org/10.1134/s1070363206060259.

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20

Leis, J. Ramón, M. Elena Peña, and Ana M. Ríos. "Nucleophilic reactivity towards ‘normal’ and ambidentate electrophiles bearing the nitroso group." J. Chem. Soc., Perkin Trans. 2, no. 3 (1995): 587–93. http://dx.doi.org/10.1039/p29950000587.

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21

Latypov, Shamil K., Yulia S. Ganushevich, Svetlana A. Kondrashova, Sergey V. Kharlamov, Vasily A. Milyukov, and Oleg G. Sinyashin. "Structural Diversity and Dynamics of Nickel Complexes with Ambidentate Phosphorus Heterocycles." Organometallics 37, no. 14 (2018): 2348–57. http://dx.doi.org/10.1021/acs.organomet.8b00319.

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22

GARNOVSKII, A. D. "ChemInform Abstract: Coordination Chemistry of Ambidentate Azole, Azomethine, and Azo Ligands." ChemInform 29, no. 31 (2010): no. http://dx.doi.org/10.1002/chin.199831282.

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23

Sheldrick, William S., and Iris M. Müller. "Alkylcycloarsoxanes and alkylcycloarsathianes—ambidentate macrocyclic ligands of variable metal-mediated ring size." Coordination Chemistry Reviews 182, no. 1 (1999): 125–73. http://dx.doi.org/10.1016/s0010-8545(98)00195-7.

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24

De Sousa, Gerimario F., Carlos A. L. Filgueiras, Marcetta Y. Darensbourg, and Joseph H. Reibenspies. "Complexation of organotin halides with ambidentate, S, N, and O donor ligands." Inorganic Chemistry 31, no. 14 (1992): 3044–49. http://dx.doi.org/10.1021/ic00040a011.

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25

Vasil'chenko, I. S., T. A. Kuz'menko, T. E. Shestakova, et al. "New Ambidentate Ligands—Azomethin Derivatives of 1-Amino-3-methylbenzimidazoline-2-thion." Russian Journal of Coordination Chemistry 31, no. 10 (2005): 747–51. http://dx.doi.org/10.1007/s11173-005-0163-6.

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26

Plebst, Sebastian, Martina Bubrin, David Schweinfurth, Stanislav Záliš, and Wolfgang Kaim. "Metal carbonyl complexes of potentially ambidentate 2,1,3-benzothiadiazole and 2,1,3-benzoselenadiazole acceptors." Zeitschrift für Naturforschung B 72, no. 11 (2017): 839–46. http://dx.doi.org/10.1515/znb-2017-0100.

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AbstractThe compounds [W(CO)5(btd)], [W(CO)5(bsd] and [Re(CO)3(bpy)(bsd)](BF4), btd=2,1,3-benzothiadiazole and bsd=2,1,3-benzoselenadiazole were isolated and characterized experimentally (crystal structure, spectroscopy, spectroelectrochemistry) and by density functional theory calculations. The results confirm single N-coordination in all cases, binding to Se was calculated to be less favorable. Studies of one-electron reduced forms indicate that the N-coordination is maintained during electron transfer.

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27

Boyce, Annemè, Thomas I. A. Gerber, and Eric C. Hosten. "Complexes of Ambidentate N,O-Donor Ligands with Rhenium(I) and -(V)." Journal of Chemical Crystallography 48, no. 3 (2018): 96–102. http://dx.doi.org/10.1007/s10870-018-0715-5.

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28

M., Sivasankaran Nair, and Subbalakshmi G. "Multiple equilibria involved in some nickel(II) mixed ligand complex systems containing catecholic and dipeptide ligands." Journal of Indian Chemical Society Vol. 77, Jan 2000 (2000): 26–28. https://doi.org/10.5281/zenodo.5861391.

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Department of Chemistry, Manonmaniam Sundaranar University, Abishekapatti, Tirunelveli-627 012, India <em>Manuscript received 10 February 1999, accepted 9 July 1999</em> Multiple equilibrium studies on Ni<sup>II</sup>-dopamineklopa(A)-glycyl-L-tryosine and L-tyrosylglycine(B) systems show the formation of NiABH<sub>2</sub>, NiABH or NiAB mixed ligand complexes. The results indicate that dopa is ambidentate, i.e. in NiABH<sub>2</sub> species it binds the metal ion in a glycine-like mode, while it coordinates in a pyrocatecholic mode in NiABH and NiAB complexes. Dopamine(A) binds in a pyrocatech

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29

Rodríguez-Rodríguez, Aurora, Zakaria Halime, Luís M. P. Lima, et al. "Cyclams with Ambidentate Methylthiazolyl Pendants for Stable, Inert, and Selective Cu(II) Coordination." Inorganic Chemistry 55, no. 2 (2015): 619–32. http://dx.doi.org/10.1021/acs.inorgchem.5b01779.

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30

López-Cardoso, Marcela, Patricia Garcı́a y Garcı́a, Alejandro Rogers-Sakuma, and Raymundo Cea-Olivares. "Organometallic tin(IV) derivatives of the ambidentate O-cholesteryl-O-phenyl phosphorothioate ligand." Polyhedron 19, no. 13 (2000): 1539–43. http://dx.doi.org/10.1016/s0277-5387(00)00396-x.

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31

Vujkovic, Nadia, Vincent César, Noël Lugan, and Guy Lavigne. "An Ambidentate Janus-Type Ligand System Based on Fused Carbene and Imidato Functionalities." Chemistry - A European Journal 17, no. 47 (2011): 13151–55. http://dx.doi.org/10.1002/chem.201102767.

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32

Walczak, Anna, Gracjan Kurpik, and Artur R. Stefankiewicz. "Intrinsic Effect of Pyridine-N-Position on Structural Properties of Cu-Based Low-Dimensional Coordination Frameworks." International Journal of Molecular Sciences 21, no. 17 (2020): 6171. http://dx.doi.org/10.3390/ijms21176171.

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Metal-organic assemblies have received significant attention for catalytic and other applications, including gas and energy storage, due to their porosity and thermal/chemical stability. Here, we report the synthesis and physicochemical characterization of three metallosupramolecular assemblies consisting of isomeric ambidentate pyridyl-β-diketonate ligands L1–L3 and Cu(II) metal ions. It has been demonstrated that the topology and dimensionality of generated supramolecular aggregates depend on the location of the pyridine nitrogen donor atom in L1–L3. This is seen in characterization of two d

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33

Homolya, L., S. Strueß, and W. Preetz. "Kristallstrukturen, Schwingungsspektren und Normalkoordinatenanalyse von cis-[ReCl4X2]2-, X = NCS, NCSe / Crystal Structures, Vibrational Spectra and Normal Coordinate Analysis of cis-[ReCl4X2]2-, X = NCS, NCSe." Zeitschrift für Naturforschung B 53, no. 11 (1998): 1329–34. http://dx.doi.org/10.1515/znb-1998-1117.

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The crystal structures of cis-(n-Bu4N)2[ReCl4(NCS)2] (triclinic, space group P1̅, a = 11,245( 1), b = 20.174(3), c = 21.320(8) Å, a =109.06(2), β = 96.46(2), γ = 98.22(5)°, Z = 4) and cis-(Ph4P)2[ReCl4(NCSe)2]·2CH2Cl2 (triclinic, space group P1̅, a = 10.341(2), b = 13.436(3), c = 19.616(4) Å, α = 92.70(2), β = 92.02(2), γ = 89.99( 1)°, Z= 2) have been determined by single crystal X-ray diffraction analysis. Both ambidentate ligands NCS and NCSe are bonded via the N atom. Using the molecular parameters of the X-ray determinations the low temperature (10 K) IR and Raman spectra of the (n-Bu4N) s

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34

N., Ravi Kumar Reddy, Bhoopal M., and Satyanarayana S. "Synthesis of thiocyanato(pyridine )cobaloximes." Journal of Indian Chemical Society Vol. 80, July 2003 (2003): 677–79. https://doi.org/10.5281/zenodo.5835358.

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Department of Chemistry, Osmania University, Hyderabad-500 007, India <em>E-mail</em> : ssnsirasani@yahoomail.com <em>Manuscript received 9 July 2002, revised 20 November 2002, accepted 31 January 2003</em> Octahedral cobalt(III) complexes are formed by the aerial oxidation of cobalt(II) salts in the presence of dimethylglyoxime and pyridines. The oximes are bonded as bidentate chelates occupying the planar positions and the complexes have <em>trans</em>-octahedral geometry with pyridines and thiocyanate in the axial positions. NMR observation suggests that in solution these compounds exist as

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35

Domasevitch, Konstantin V., Victor V. Skopenko, and Eduard B. Rusanov. "Synthesis, Infrared and X-Ray Studies of Diphenyltellurium(IV) Nitrosocarbamylcyanmethanides. X-Ray Evidence for Stability of a Tritelluroxane Fragment -Ph2Te-O-Ph2Te-O-Ph2Te-." Zeitschrift für Naturforschung B 51, no. 6 (1996): 832–37. http://dx.doi.org/10.1515/znb-1996-0613.

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Abstract Diphenyltellurium(IV) derivatives of the types Ph2Te{ACO}2 (1), Ph4Te2O{ACO}2 (2) and Ph6Te3O2{ACO} (3) (ACO = nitrosocarbamylcyanmethanide -ONC(CN)C(O)NH2) have been prepared. The IR spectroscopic data reveal that the ambidentate ligands are coordinated to the tellurium(IV) atom in a monodentate manner via the nitroso oxygen atom. The crystal and molecular structure of 3 has been determined from X-ray diffraction data (triclinic, space group P1̅ with a = 12.382(2), 6=13.100(2), c = 14.944(3) Å, a = 87.74( 1), β = 85.04(2), 7 = 66.29( 1)°, V = 2211.0 A , Z = 2, R = 0.040). The structu

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36

Börner, Martin, Laura Blömer, Marcus Kischel, et al. "Deposition of exchange-coupled dinickel complexes on gold substrates utilizing ambidentate mercapto-carboxylato ligands." Beilstein Journal of Nanotechnology 8 (July 5, 2017): 1375–87. http://dx.doi.org/10.3762/bjnano.8.139.

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The chemisorption of magnetically bistable transition metal complexes on planar surfaces has recently attracted increased scientific interest due to its potential application in various fields, including molecular spintronics. In this work, the synthesis of mixed-ligand complexes of the type [NiII 2L(L’)](ClO4), where L represents a 24-membered macrocyclic hexaazadithiophenolate ligand and L’ is a ω-mercapto-carboxylato ligand (L’ = HS(CH2)5CO2 − (6), HS(CH2)10CO2 − (7), or HS(C6H4)2CO2 − (8)), and their ability to adsorb on gold surfaces is reported. Besides elemental analysis, IR spectroscop

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37

Ponomareva, Vera V., N. Kent Dalley, Xiaolan Kou, Nikolay N. Gerasimchuk, and Konstantin V. Domasevitch. "Synthesis, spectra and crystal structures of complexes of ambidentate C6H5C(O)C(NO)CN?" Journal of the Chemical Society, Dalton Transactions, no. 11 (1996): 2351. http://dx.doi.org/10.1039/dt9960002351.

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38

César, Vincent, Valentina Mallardo, Adela Nano, et al. "Homo- and Heteropolymetallic Complexes of the Hybrid, Ambidentate N-Heterocyclic Carbene Ligand IMes-acac." ACS Omega 3, no. 11 (2018): 15582–91. http://dx.doi.org/10.1021/acsomega.8b02268.

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39

de Sousa, Gerimário F., and Carlos A. L. Filgueiras. "Complexes with ambidentate ligands derived from pyridine and pyrimidine-Part 2. Platinum(II) complexes." Transition Metal Chemistry 15, no. 4 (1990): 290–92. http://dx.doi.org/10.1007/bf01061936.

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40

Sheldrick, William S., and Iris M. Mueller. "ChemInform Abstract: Alkylcycloarsoxanes and Alkylcycloarsathianes - Ambidentate Macrocyclic Ligands of Variable Metal-Mediated Ring Size." ChemInform 30, no. 19 (2010): no. http://dx.doi.org/10.1002/chin.199919300.

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41

Kia, Reza, Shiva Batmanghelich та Paul R. Raithby. "First heterobimetallic AgI–CoIII coordination compound with both bridging and terminal –NO2 coordination modes: synthesis, characterization, structural and computational studies of (PPh3)2AgI–(μ-κ2 O,O′:κN-NO2)–CoIII(DMGH)2(κN-NO2)". Acta Crystallographica Section C Structural Chemistry 74, № 8 (2018): 882–88. http://dx.doi.org/10.1107/s2053229618009257.

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An unusual heterobimetallic bis(triphenylphosphane)(NO2)AgI–CoIII(dimethylglyoximate)(NO2) coordination compound with both bridging and terminal –NO2 (nitro) coordination modes has been isolated and characterized from the reaction of [CoCl(DMGH)2(PPh3)] (DMGH2 is dimethylglyoxime or N,N′-dihydroxybutane-2,3-diimine) with excess AgNO2. In the title compound, namely bis(dimethylglyoximato-1κ2 O,O′)(μ-nitro-1κN:2κ2 O,O′)(nitro-1κN)bis(triphenylphosphane-2κP)cobalt(III)silver(I), [AgCo(C4H7N2O2)2(NO2)2(C18H15P)2], one of the ambidentate –NO2 ligands, in a bridging mode, chelates the AgI atom in an

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42

Kutniewska, Sylwia E., Adam Krówczyński, Radosław Kamiński, et al. "Photocrystallographic and spectroscopic studies of a model (N,N,O)-donor square-planar nickel(II) nitro complex: in search of high-conversion and stable photoswitchable materials." IUCrJ 7, no. 6 (2020): 1188–98. http://dx.doi.org/10.1107/s205225252001307x.

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A new, cheap, easy-to-synthesize and air-stable photoswitchable nickel(II) complex, QTNiNO2, is reported. The metal centre in QTNiNO2 is coordinated by a nitro group and a [2-methyl-8-aminoquinoline]-1-tetralone ligand. The compound crystallizes in the tetragonal space group I41/a with one complex molecule comprising the asymmetric unit, and the crystals are stable under ambient conditions. Irradiation of the solid-state form of QTNiNO2 with 530–660 nm LED light at 160 K converts the ambidentate nitro moiety fully to the nitrito linkage isomer which is stable up to around 230 K, as indicated b

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43

Yilmaz, Veysel T., Vecdi Kars, and Canan Kazak. "Synthesis and Characterization of Cadmium and Mercury Saccharinate Complexes with 2-Dimethylaminoethanol: cis-[Cd(sac)2(dmea)2] and [Hg(sac)2(dmea)(H2O)]." Zeitschrift für Naturforschung B 61, no. 5 (2006): 555–59. http://dx.doi.org/10.1515/znb-2006-0508.

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The new cadmium and mercury saccharinate (sac) complexes, cis-[Cd(sac)2(dmea)2] (1) and [Hg(sac)2(dmea)(H2O)] (2) (dmea = 2-dimethylaminoethanol), have been prepared and characterized by elemental analysis, IR spectroscopy, thermal analysis and single crystal X-ray diffraction. In complex 1, the cadmium(II) ion is coordinated by two neutral dmea ligands and two sac anions in a distorted octahedral CdN3O3 coordination geometry. The dmea ligand acts as a bidentate N, O chelate, while the sac ligands behave as an ambidentate ligands. One of them coordinates to the cadmium(II) ion through the carb

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44

G., N. MUKHERJEE, and K. GHOSH T. "Metal Ion Interactions with some Antibiotic Drugs of Penicillin Family. Part-IV. Equilibrium Study on the Complex Formation of Cobalt(II), Nickel(II) and Zinc(II) with Ampicillin." Journal of Indian Chemical Society Vol. 71, April 1994 (1994): 169–73. https://doi.org/10.5281/zenodo.5894207.

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Department of Chemistry, University College of Science, 92 Acharya Prafulla Chandra Road, Calcutta-700 009 Department of Chemistry, R. K. Mission Vivekananda Centenary College: Rahara-743 186 <em>Manuscript received 16 April 1993, accepted 1 June 1993</em> Combined pH-metric and spectrophotometric study on the complex formation of M<sup>2+</sup> ions (M = Co, Ni and Zn) with ampicillin, (<em>\(\alpha\)</em>-<em>d-</em>(-)aminobenzylpenicillin), ampH<sup>±</sup> at 37º in aqueous solution at a fixed ionic strength, I = 0.1 M NaN0<sub>3</sub>, provided evidence of formation

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Filippou, Vasileios, Svenja Blickle, Martina Bubrin, and Wolfgang Kaim. "Intramolecular Charge Transfer in Ruthenium Complexes [Ru(acac) 2 (ciq)] with Ambidentate Camphoriminoquinone (ciq) Ligands." Zeitschrift für anorganische und allgemeine Chemie 647, no. 5 (2021): 525–33. http://dx.doi.org/10.1002/zaac.202000464.

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Bailey, Philip J., Michele Melchionna, and Simon Parsons. "Ambidentate Character of the 6-Aminofulvene-2-aldiminate Ligand Containing Both Diimine and Cyclopentadienyl Donors." Organometallics 26, no. 1 (2007): 128–35. http://dx.doi.org/10.1021/om060808d.

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Burlov, A. S., A. S. Antsyshkina, G. G. Sadkov, et al. "Coordination compounds of ambidentate 1-(H)alkyl-2-(2-pyridyl)benzimidazoles. Synthesis and crystal structure." Russian Journal of Coordination Chemistry 36, no. 12 (2010): 906–12. http://dx.doi.org/10.1134/s1070328410120079.

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Anderson, James S. M., and Paul W. Ayers. "Predicting the reactivity of ambidentate nucleophiles and electrophiles using a single, general-purpose, reactivity indicator." Physical Chemistry Chemical Physics 9, no. 19 (2007): 2371. http://dx.doi.org/10.1039/b700960g.

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Johansson, Olof, and Reiner Lomoth. "Molecular Hysteresis in a Rigid Dinuclear Ruthenium Polypyridyl Complex Incorporating a Ligand-Bound Ambidentate Motif." Inorganic Chemistry 47, no. 13 (2008): 5531–33. http://dx.doi.org/10.1021/ic800075b.

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Goodgame, David M. L., David A. Grachvogel, Andrew J. P. White, and David J. Williams. "Diverse polymeric metal complexes formed by the ambidentate ligand 1-(4′-pyridyl)pyridin-4-one." Inorganica Chimica Acta 348 (May 2003): 187–93. http://dx.doi.org/10.1016/s0020-1693(02)01473-1.

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