"Coordination Complexes" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Neutral or negatively charged ligands bonded to metal cations or neutral atoms. The number of ligand atoms to which the metal center is directly bonded is the metal cation's coordination number, and this number is always greater than the regular valence or oxidation number of the metal. A coordination complex can be negative, neutral, or positively charged.
| Descriptor ID |
D056831
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| MeSH Number(s) |
D01.234 D02.691.214
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| Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Coordination Complexes".
Below are MeSH descriptors whose meaning is more specific than "Coordination Complexes".
This graph shows the total number of publications written about "Coordination Complexes" by people in this website by year, and whether "Coordination Complexes" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2004 | 0 | 1 | 1 |
| 2010 | 1 | 0 | 1 |
| 2011 | 0 | 1 | 1 |
| 2013 | 2 | 1 | 3 |
| 2014 | 1 | 1 | 2 |
| 2020 | 0 | 1 | 1 |
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Below are the most recent publications written about "Coordination Complexes" by people in Profiles.
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Wang D, Farnum BH, Dares CJ, Meyer TJ. Chemical approaches to artificial photosynthesis: A molecular, dye-sensitized photoanode for O2 production prepared by layer-by-layer self-assembly. J Chem Phys. 2020 Jun 28; 152(24):244706.
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Singh P, Aggarwal S, Tiwari AK, Kumar V, Pratap R, Chuttani K, Mishra AK. Bis(methylpyridine)-EDTA derivative as a potential ligand for PET imaging: synthesis, complexation, and biological evaluation. Chem Biol Drug Des. 2014 Dec; 84(6):704-11.
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Song N, Zhang MT, Binstead RA, Fang Z, Meyer TJ. Multiple pathways in the oxidation of a NADH analogue. Inorg Chem. 2014 Apr 21; 53(8):4100-5.
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Concepcion JJ, Binstead RA, Alibabaei L, Meyer TJ. Application of the rotating ring-disc-electrode technique to water oxidation by surface-bound molecular catalysts. Inorg Chem. 2013 Oct 07; 52(19):10744-6.
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Lau EY, Wong SE, Baker SE, Bearinger JP, Koziol L, Valdez CA, Satcher JH, Aines RD, Lightstone FC. Comparison and analysis of zinc and cobalt-based systems as catalytic entities for the hydration of carbon dioxide. PLoS One. 2013; 8(6):e66187.
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Brennaman MK, Fleming CN, Slate CA, Serron SA, Bettis SE, Erickson BW, Papanikolas JM, Meyer TJ. Distance dependence of intrahelix Ru(II)* to Os(II) polypyridyl excited-state energy transfer in oligoproline assemblies. J Phys Chem B. 2013 May 30; 117(21):6352-63.
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Meyer TJ. Catalysis: oxidizing water two ways. Nat Chem. 2011 Sep 23; 3(10):757-8.
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Van Heuvelen KM, Cho J, Dingee T, Riordan CG, Brunold TC. Spectroscopic and computational studies of a series of high-spin Ni(II) thiolate complexes. Inorg Chem. 2010 Jul 19; 49(14):6535-44.
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Striplin DR, Reece SY, McCafferty DG, Wall CG, Friesen DA, Erickson BW, Meyer TJ. Solvent dependence of intramolecular electron transfer in a helical oligoproline assembly. J Am Chem Soc. 2004 Apr 28; 126(16):5282-91.