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1

Salzer, A. "Nomenclature of Organometallic Compounds of the Transition Elements (IUPAC Recommendations 1999)." Pure and Applied Chemistry 71, no. 8 (1999): 1557–85. http://dx.doi.org/10.1351/pac199971081557.

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Organometallic compounds are defined as containing at least one metal-carbon bond between an organic molecule, ion, or radical and a metal. Organometallic nomenclature therefore usually combines the nomenclature of organic chemisty and that of coordination chemistry. Provisional rules outlining nomenclature for such compounds are found both in Nomenclature of Organic Chemistry, 1979 and in Nomenclature of Inorganic Chemistry, 1990This document describes the nomenclature for organometallic compounds of the transition elements, that is compounds with metal-carbon single bonds, metal-carbon multi
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2

Kelling, Leif, and Viktoria H. Gessner. "Coordination chemistry of a weakly coordinating carbanion." Polyhedron 265 (January 2025): 117283. http://dx.doi.org/10.1016/j.poly.2024.117283.

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3

Wenger, Marc, and Thomas Armbruster. "Crystal chemistry of lithium: oxygen coordination and bonding." European Journal of Mineralogy 3, no. 2 (1991): 387–400. http://dx.doi.org/10.1127/ejm/3/2/0387.

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4

Porras Gutiérrez, Ana Gabriela, Joceline Zeitouny, Antoine Gomila, et al. "Insights into water coordination associated with the CuII/CuI electron transfer at a biomimetic Cu centre." Dalton Trans. 43, no. 17 (2014): 6436–45. http://dx.doi.org/10.1039/c3dt53548g.

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5

Hindson, Karen. "Coordination Chemistry." European Journal of Inorganic Chemistry 2012, no. 29 (2012): 4519. http://dx.doi.org/10.1002/ejic.201290090.

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6

Delanoue, Renald, and Nuria M. Romero. "Growth and Maturation in Development: A Fly’s Perspective." International Journal of Molecular Sciences 21, no. 4 (2020): 1260. http://dx.doi.org/10.3390/ijms21041260.

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In mammals like humans, adult fitness is improved due to resource allocation, investing energy in the developmental growth process during the juvenile period, and in reproduction at the adult stage. Therefore, the attainment of their target body height/size co-occurs with the acquisition of maturation, implying a need for coordination between mechanisms that regulate organismal growth and maturation timing. Insects like Drosophila melanogaster also define their adult body size by the end of the juvenile larval period. Recent studies in the fly have shown evolutionary conservation of the regula
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7

Herberhold, Max, and Anthony F. Hill. "The coordination chemistry of iminooxosulphuranes VII. Coordinative activation of tolyliminooxosulphurane towards electrophiles." Journal of Organometallic Chemistry 395, no. 2 (1990): 207–18. http://dx.doi.org/10.1016/0022-328x(90)85278-7.

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8

Krezel, A., and W. Bal. "Coordination chemistry of glutathione." Acta Biochimica Polonica 46, no. 3 (1999): 567–80. http://dx.doi.org/10.18388/abp.1999_4129.

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The metal ion coordination abilities of reduced and oxidized glutathione are reviewed. Reduced glutathione (GSH) is a very versatile ligand, forming stable complexes with both hard and soft metal ions. Several general binding modes of GSH are described. Soft metal ions coordinate exclusively or primarily through thiol sulfur. Hard ones prefer the amino acid-like moiety of the glutamic acid residue. Several transition metal ions can additionally coordinate to the peptide nitrogen of the gamma-Glu-Cys bond. Oxidized glutathione lacks the thiol function. Nevertheless, it proves to be a surprising
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9

Lusby, Paul J. "Supramolecular coordination chemistry." Annual Reports Section "A" (Inorganic Chemistry) 108 (2012): 292. http://dx.doi.org/10.1039/c2ic90030k.

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10

Archibald, Stephen J. "Macrocyclic coordination chemistry." Annual Reports Section "A" (Inorganic Chemistry) 108 (2012): 271. http://dx.doi.org/10.1039/c2ic90035a.

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11

Lusby, Paul J. "Supramolecular coordination chemistry." Annual Reports Section "A" (Inorganic Chemistry) 105 (2009): 323. http://dx.doi.org/10.1039/b818282p.

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12

Archibald, Stephen J. "Macrocyclic coordination chemistry." Annual Reports Section "A" (Inorganic Chemistry) 102 (2006): 332. http://dx.doi.org/10.1039/b514842c.

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13

Cronin, Leroy. "Supramolecular coordination chemistry." Annual Reports Section "A" (Inorganic Chemistry) 102 (2006): 353. http://dx.doi.org/10.1039/b514843j.

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14

Kostakis, George E., and Sally Brooker. "Modern coordination chemistry." Dalton Transactions 48, no. 41 (2019): 15318–20. http://dx.doi.org/10.1039/c9dt90209k.

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15

Archibald, Stephen J. "Macrocyclic coordination chemistry." Annual Reports Section "A" (Inorganic Chemistry) 106 (2010): 295. http://dx.doi.org/10.1039/b918391b.

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16

Lusby, Paul J. "Supramolecular coordination chemistry." Annual Reports Section "A" (Inorganic Chemistry) 106 (2010): 319. http://dx.doi.org/10.1039/b918392m.

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17

Archibald, Stephen J. "Macrocyclic coordination chemistry." Annual Reports Section "A" (Inorganic Chemistry) 103 (2007): 264. http://dx.doi.org/10.1039/b612865n.

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18

Pradeep, Chullikkattil P., and Leroy Cronin. "Supramolecular coordination chemistry." Annual Reports Section "A" (Inorganic Chemistry) 103 (2007): 287. http://dx.doi.org/10.1039/b612867j.

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19

Archibald, Stephen J. "Macrocyclic coordination chemistry." Annual Reports Section "A" (Inorganic Chemistry) 104 (2008): 272. http://dx.doi.org/10.1039/b716584f.

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20

Lusby, Paul J. "Supramolecular coordination chemistry." Annual Reports Section "A" (Inorganic Chemistry) 104 (2008): 297. http://dx.doi.org/10.1039/b716586m.

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21

Lusby, Paul J. "Supramolecular coordination chemistry." Annual Reports Section "A" (Inorganic Chemistry) 109 (2013): 254. http://dx.doi.org/10.1039/c3ic90025h.

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22

Burke, Benjamin P., and Stephen J. Archibald. "Macrocyclic coordination chemistry." Annual Reports Section "A" (Inorganic Chemistry) 109 (2013): 232. http://dx.doi.org/10.1039/c3ic90032k.

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23

Lusby, Paul J. "Supramolecular coordination chemistry." Annual Reports Section "A" (Inorganic Chemistry) 107 (2011): 297. http://dx.doi.org/10.1039/c1ic90026a.

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24

Archibald, Stephen J. "Macrocyclic coordination chemistry." Annual Reports Section "A" (Inorganic Chemistry) 107 (2011): 274. http://dx.doi.org/10.1039/c1ic90033a.

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25

Seddon, K. R. "Coordination Chemistry reviews." Coordination Chemistry Reviews 89 (September 1988): vii. http://dx.doi.org/10.1016/0010-8545(88)80035-3.

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26

Wong, Chih Y., and J. D. Woollins. "Beryllium coordination chemistry." Coordination Chemistry Reviews 130, no. 1-2 (1994): 243–73. http://dx.doi.org/10.1016/0010-8545(94)80006-5.

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27

Eaborn, Colin. "Comprehensive Coordination Chemistry." Journal of Organometallic Chemistry 356, no. 2 (1988): C65. http://dx.doi.org/10.1016/0022-328x(88)83103-6.

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28

Keep, Ann K. "Expanded Coordination Chemistry." Platinum Metals Review 48, no. 2 (2004): 64–65. http://dx.doi.org/10.1595/003214004x4826465.

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29

J., C.TREHAN, R.K.SHARMA, KUMAR N., P. SHARMA C., S. GARG B. та P. SINGH R. "Spectroscopic Studies of some New Diorganotin(IV)- β-diketonate Complexes". Journal of Indian Chemical Society Vol. 62, Oct 1985 (1985): 777–78. https://doi.org/10.5281/zenodo.6324692.

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National Physical Laboratory, Hillside Road, New Delhi-110 012 Department of Chemistry, University of Delhi, Delhi-110 007 <em>Manuscript received 26 June 1984, revised 30&nbsp;April 1985, accepted 29 October 1985</em> Spectroscopic Studies of some New Diorganotin(IV)- <em>&beta;</em>-diketonate Complexes &nbsp;
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30

Md Mohiuddin and Md Azharul Arafath, Md Mohiuddin and Md Azharul Arafath. "Coordination Complexes of Copper, Silver and Gold with SNO Group Containing Thiosemicarbazones Schiff Base Ligands and their Biological Applications." Journal of the chemical society of pakistan 46, no. 1 (2024): 52. http://dx.doi.org/10.52568/001422/jcsp/46.01.2024.

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The thiosemicarbazone Schiff base ligand is very important segment for chemistry, more specifically coordination chemistry. These compounds and their complexes widely used as medicinal agents for different lethal diseases such as cancer and other contagious disease caused by bacteria. The coordinated metal (coinage) complexes exhibited higher activities than free ligand for all the biological investigation of anticancer and antibacterial activities. The TSCs ligands having polydentate S-N-O coordinating sites. The mode of coordination of these ligands is flexible, it can act as tridentate or b
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31

Taakili, Rachid, and Yves Canac. "NHC Core Pincer Ligands Exhibiting Two Anionic Coordinating Extremities." Molecules 25, no. 9 (2020): 2231. http://dx.doi.org/10.3390/molecules25092231.

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The chemistry of NHC core pincer ligands of LX2 type bearing two pending arms, identical or not, whose coordinating center is anionic in nature, is here reviewed. In this family, the negative charge of the coordinating atoms can be brought either by a carbon atom via a phosphonium ylide (R3P+–CR2−) or by a heteroatom through amide (R2N−), oxide (RO−), or thio(seleno)oxide (RS−, RSe−) donor functionalities. Through selected examples, the synthetic methods, coordination properties, and applications of such tridentate systems are described. Particular emphasis is placed on the role of the donor e
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32

Zheng, Heping, Mahendra Chordia, David Cooper, et al. "Check your metal - not every density blob is a water molecule." Acta Crystallographica Section A Foundations and Advances 70, a1 (2014): C1483. http://dx.doi.org/10.1107/s2053273314085167.

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Metals play vital roles in both the mechanism and architecture of biological macromolecules, and are the most frequently encountered ligands (i.e. non-solvent heterogeneous chemical atoms) in the determination of macromolecular crystal structures. However, metal coordinating environments in protein structures are not always easy to check in routine validation procedures, resulting in an abundance of misidentified and/or suboptimally modeled metal ions in the Protein Data Bank (PDB). We present a solution to identify these problems in three distinct yet related aspects: (1) coordination chemist
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33

Meyer, Michel, Claude P. Gros, and Laurent Plasseraud. "Equilibrium solution coordination chemistry." New Journal of Chemistry 42, no. 10 (2018): 7514–15. http://dx.doi.org/10.1039/c8nj90042f.

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34

Kanaoujiya, Rahul, and Shekhar Srivastava. "Coordination Chemistry of Ruthenium." Research Journal of Chemistry and Environment 25, no. 9 (2021): 103–6. http://dx.doi.org/10.25303/259rjce103106.

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Ruthenium is one of the rare elements that belongs to the platinum group metals. Ruthenium is very effective hardener for platinum and palladium. Well studied coordination and organometallic chemistry of ruthenium results in a various varieties of compounds. There are various features of ruthenium such as oxidation states, coordination numbers and geometries. Ruthenium compounds have various applications and also have low toxicity and they are ideal for the catalytic synthesis of drugs. The field of ruthenium chemistry is very broad and is extremely diverse in the field of catalysis and medici
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35

D., Kumar, Sharma Jyoti, Chadda Silky, and Syamal A. "Syntheses and characterization of the coordination compounds of metal ions of first and second transition series with the Schiff base in aqueous and non-aqueous reaction conditions." Journal of Indian Chemical Society Vol. 90, Aug 2013 (2013): 1077–86. https://doi.org/10.5281/zenodo.5783501.

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Department of Chemistry, National Institute of Technology, Kurukshetra-136 119, Haryana, India E-mail : dkumar_nitk@yahoo.com, silkychadda2010@gmail.com Department of Chemistry, International Institute of Engineering and Technology, Samani, Kurukshetra-136 118, Haryana, India E-mail : sharadpr123@rediffmail.com SchooI&nbsp;of Coordination Chemistry, D Wing, Ushanagar, Bhandup, Mumbai-400 078, India <em>E-mail :</em> arunsyamal@yahoo.co.in <em>Manuscript received online 05 October 2012, revised 19 October 2012, accepted 25 October 2012</em> The coordination compounds of some metal ions of first
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36

Comba, Peter, Aldo Hörmann, Lisandra L. Martin, and Luc Zipper. "Stereoselective Coordination to Chiral Matrices. Cobalt(III). Chemistry of Simple Facially Coordinating Chiral Triamines." Helvetica Chimica Acta 73, no. 4 (1990): 874–82. http://dx.doi.org/10.1002/hlca.19900730413.

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37

Lipunova, G. N., T. G. Fedorchenko, and O. N. Chupakhin. "Verdazyls in Coordination Chemistry." Russian Journal of Coordination Chemistry 48, no. 7 (2022): 397–411. http://dx.doi.org/10.1134/s1070328422070065.

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38

Ward, M. D. "18 Supramolecular coordination chemistry." Annual Reports Section "A" (Inorganic Chemistry) 96 (2000): 345–85. http://dx.doi.org/10.1039/b002989k.

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39

Carter, Timothy G., W. Jake Vickaryous, Virginia M. Cangelosi, and Darren W. Johnson. "SUPRAMOLECULAR ARSENIC COORDINATION CHEMISTRY." Comments on Inorganic Chemistry 28, no. 3-4 (2007): 97–122. http://dx.doi.org/10.1080/02603590701560994.

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40

Gubin, S. P., and N. A. Kataeva. "Coordination chemistry of nanoparticles." Russian Journal of Coordination Chemistry 32, no. 12 (2006): 849–57. http://dx.doi.org/10.1134/s1070328406120013.

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41

Ward, M. D. "18 Supramolecular coordination chemistry." Annu. Rep. Prog. Chem., Sect. A: Inorg. Chem. 98 (2002): 285–320. http://dx.doi.org/10.1039/b109632j.

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42

Sachdev, Hermann, Christian Wagner, Cordula Preis, Volker Huch, and Michael Veith. "Coordination chemistry of furfurylsilylamides." Journal of the Chemical Society, Dalton Transactions, no. 24 (November 22, 2002): 4709–13. http://dx.doi.org/10.1039/b205350k.

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43

Inoue, Shigeyoshi. "Coordination Chemistry of Silicon." Inorganics 7, no. 1 (2019): 7. http://dx.doi.org/10.3390/inorganics7010007.

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44

BRESSAN, M., R. ETTORRE, F. MARCHIORI, and G. VALLE. "Coordination chemistry of peptides." International Journal of Peptide and Protein Research 19, no. 4 (2009): 402–7. http://dx.doi.org/10.1111/j.1399-3011.1982.tb02621.x.

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45

Arduengo, Anthony J., H. V. Rasika Dias, and J. C. Calabrese. "Coordination Chemistry of ADPO." Phosphorus, Sulfur, and Silicon and the Related Elements 87, no. 1-4 (1994): 1–10. http://dx.doi.org/10.1080/10426509408037435.

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46

Cupertino, Dominico, Robin Keyte, Alexandra Slawin, David Williams, and J. Derek Woollins. "Coordination Chemistry of Dithioimidophosphinates." Phosphorus, Sulfur, and Silicon and the Related Elements 109, no. 1 (1996): 193–96. http://dx.doi.org/10.1080/10426509608046231.

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47

Cupertino, Dominico, Robin W. Keyte, Alexandra M. Z. Slawin, David J. Williams, and J. Derek Woollins. "Coordination Chemistry of Dithioimidophosphinates." Phosphorus, Sulfur, and Silicon and the Related Elements 109, no. 1-4 (1996): 193–96. http://dx.doi.org/10.1080/10426509608545123.

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48

Vedernikov, Andrei N., John C. Huffman, and Kenneth G. Caulton. "Coordination Chemistry of Tripyridinedimethane." Inorganic Chemistry 41, no. 24 (2002): 6244–48. http://dx.doi.org/10.1021/ic025708o.

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49

Peng, S. M., and M. C. Liaw. "Trigonal prismatic coordination chemistry." Acta Crystallographica Section A Foundations of Crystallography 49, s1 (1993): c228. http://dx.doi.org/10.1107/s0108767378093629.

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50

Abdelhalim Ahmed, Ibrahim, Guido Kastner, Hans Reuter, and Dietrich Schultze. "Coordination chemistry of tin." Journal of Organometallic Chemistry 649, no. 2 (2002): 147–51. http://dx.doi.org/10.1016/s0022-328x(02)01111-7.

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