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| Coordination = ...]] manufacture.<ref name="holleman">Holleman, A. F.; Wiberg, E. "Inorganic Chemistry" Academic Press: San Diego, 2001. ISBN 0-12-352651-5</ref> In the laborato

...ion|adverse effect]]s include drowsiness, headaches and migraines, [[motor coordination]] impairment and/or upset stomach. Carbamazepine preparations typically gre ==Chemistry==

| Coordination = ...yday "Iodine and Iodine Compounds" in Ullmann's Encyclopedia of Industrial Chemistry, 2005, Wiley-VCH, Weinheim</ref>

| Coordination = ...t5 = M.B.P.P. | last6 = Delerue-Matos | first6 = Cristina | journal = Food Chemistry | volume = 120 | pages = 960}}</ref><ref name = Leszczyńska>{{cite journa

| Coordination = ...lleman: [http://books.google.com/books?id=vEwj1WZKThEC&pg=PA1444 Inorganic chemistry], p.1444. Academic Press, 2001; Google books</ref><br />

| Coordination = ...function of frequency. Lower frequencies are less affected by the [[Salt (chemistry)|salt]], so that the acoustic energy travels much farther in the ocean. [[B

...behavioural testing has shown normal functioning on perception, cognition, coordination and behaviour in most cases. One recent study<ref>{{cite journal |author=Ga ==Chemistry==

...liəm|}}) by [[Hoffmann-La Roche]], is a [[benzodiazepine]] [[derivative (chemistry)|derivative]] [[drug]]. It is commonly used for treating [[anxiety]], [[ins ** Impaired coordination

| Coordination = Octahedral (Na⁺)<br/>Octahedral (Cl^–) ...ula|formula]] [[Sodium|Na]][[Chloride|Cl]]. Sodium chloride is the [[salt (chemistry)|salt]] most responsible for the salinity of the [[ocean]] and of the [[ext

...Acid and Related Chelating Agents" in Ullmann's Encyclopedia of Industrial Chemistry, Wiley-VCH, Weinheim, 2005.{{DOI|10.1002/14356007.a10_095}}</ref> ...ate base]] that is the [[ligand]], and H₄EDTA, the [[precursor (chemistry)|precursor]] to that ligand. At very low pH (very acidic conditions) the f

...R>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;of&nbsp;Life || '''3.2.1'''&nbsp;[[Organic chemistry|Chemicals&nbsp;and&nbsp;the&nbsp;Vital&nbsp;Processes]] '''3.2.2'''&nbsp;[[ ...Physiology|Function&nbsp;in&nbsp;Organisms]] '''3.3.3'''&nbsp;[[Homostasis|Coordination&nbsp;of&nbsp;Vital&nbsp;Processes:&nbsp;Regulation&nbsp;and&nbsp;Integratio

| Coordination = Acrylates and acrylic chemistry have a wide variety of industrial uses that include:

...]. Non-covalent forces that hold supramolecular polymers together include coordination, π-π interactions, and hydrogen bonding. One system that has been demons [[Category:Supramolecular chemistry]]

...an scientific fields such as [[Organic chemistry|organic]] and [[inorganic chemistry]], [[biology]], [[materials science]], [[electrochemistry]], and pharmacolo Coordination polymers can be classified in a number of different ways due to particular

...ments such as [[silicon]] form familiar materials such as [[silicones]]. [[Coordination polymer]]s may contain a range of metals in the backbone, with non-covalent *[[RAFT (chemistry)]]

...ounds (Recommendations 1993)] IUPAC, Commission on Nomenclature of Organic Chemistry, 1993, Blackwell Scientific</ref>). The difference in names between the two ...]], [[anionic addition polymerization]], [[Coordination polymerization|ion coordination polymerization]] or [[cationic addition polymerization]]. This is because e

As chemistry developed into a science it became clear that metals formed the large major ...ment holds. It has very similar properties to benzene.<ref name=Greenwood>>Chemistry of the elements, N.N. Greenwood A. Earnshaw. Pergamon Press 1984 ISBN 0-08-

...a powder.<ref name=cotton>{{cite book|last = Cotton|first = Simon|title = Chemistry of Precious Metals| pages = 1–20|publisher = Springer-Verlag New York, LL ...s from Spent Nuclear Fuel. Part I PART I: General Considerations and Basic Chemistry|url =http://www.platinummetalsreview.com/pdf/pmr-v47-i2-074-087.pdf| first1

...c dialkyldithiophosphates''' (often referred to as ZDDP) are a family of [[coordination compound]]s that feature [[zinc]] bound to the anion of dithiophosphoric ac ==Coordination chemistry==

==Chemistry and compounds==

| Coordination = ...Phenylene- and Toluenediamines” in Ullmann's Encyclopedia of Industrial Chemistry 2002, Wiley-VCH, Weinheim. {{DOI|10.1002/14356007.a19_405}}</ref>

| Coordination = ...OH. Typically available as a white powder,<ref name=crc>[[CRC Handbook of Chemistry and Physics]] 65th Ed.</ref> it is commonly used as a developer in [[black

| Coordination = ...dat, Dieter Mayer "Ethylene Oxide" in Ullmann's Encyclopedia of Industrial Chemistry Wiley-VCH, Weinheim, 2005.{{DOI|10.1002/14356007.a10_117}}.</ref>

...tic susceptibility of the elements and inorganic compounds, in Handbook of Chemistry and Physics| publisher = CRC press| isbn = 0849304857|first = David R. last ...elative to other oxidation states of manganese.<ref>'''Descriptive Organic Chemistry''' Geoffrey Rayner-Canham, Tina Overton, Macmillan, 2003. p. 491</ref>

Many of these issues have required the coordination over a number of years of a number of medical and para professionals in det **Basic Sciences (Biology, Chemistry, Mathematics (Statistics), Physics);

...er some time, due to the substitution of water for chloride in the inner [[coordination sphere]]. This kind of reaction is also observed in [[chrome alum]] solutio {{Main|organochromium chemistry}}

...) is a medical condition caused by increased levels of the [[Heavy metal (chemistry)|heavy metal]] [[lead]] in the body. Lead interferes with a variety of body ...tration, [[depression (mood)|depression]], nausea, abdominal pain, loss of coordination, and numbness and tingling in the extremities.<ref name="Patrick06"/> Fati

...ate complex''' with the substrate. Chelate complexes are contrasted with [[coordination complex]]es with [[Denticity|monodentate]] ligands, which form only one bon [[Image:Cu chelate.png|thumb|Cu²⁺ [[Coordination complex|complexes]] with [[methylamine]] (left) ''and'' [[ethylenediamine]]

...₂ is used in the analysis of [[palladium]] or [[nickel]]. Its [[coordination complex]]es are of theoretical interest as models for enzymes and as cataly ...hfuss, T.B.; Angelici, R. J.| title = Synthesis and Technique in Inorganic Chemistry: A Laboratory Manual | edition = 3rd | date = 1999 | pages = 213–215 }}</

...menko, '''Scorpionates: Polypyrazolylborate Ligands and Their Coordination Chemistry'''. World Scientific Publishing Company, 1999.</ref> <ref>[[Chemical & Engi ...eteroscorpionate Ligands of Relevance to Molybdoenzymes, (2004), Inorganic Chemistry]</ref>.

| title = Handbook of Chemistry and Physics ...[[pyridine]]. This colourless solid is used as a ligand in [[coordination chemistry]].

...ng field of [[supramolecular chemistry]].<ref>Lehn, J. M. ''Supramolecular Chemistry: Concepts and Perspectives''; VCH: Weinhiem, 1995.</ref> The term cryptand ...ub>3</sub>N; the formal [[IUPAC]] (International Union of Pure and Applied Chemistry) name for this compound is 1,10-diaza-4,7,13,16,21,24-hexaoxabicyclo[8.8.8]

...lfried Paulus "Phenol Derivatives" in Ullmann's Encyclopedia of Industrial Chemistry, Wiley-VCH, 2002: Weinheim. DOI: 10.1002/14356007.a19_313. Article Online P ===Organic chemistry===

...mistry]], it forms strong complexes with most metal ions. In terms of its coordination properties, phen is similar to [[2,2'-bipyridine]] (bipy). ...Application of chelate Compounds in Analytical Chemistry" Pure and Applied Chemistry, 1973, volume 34, pages 13-27.</ref> It is used as a [[redox]] [[redox ind

...Hartmut Höke "Amines, Aliphatic" in Ullmann's Encyclopedia of Industrial Chemistry, 2005 Wiley-VCH Verlag, Weinheim. {{DOI:10.1002/14356007.a02_001}}</ref> .... Ethylenediamine is a well-known [[chelation|chelating]] [[ligand]] for [[coordination compound]]s, such as [[Tris(ethylenediamine)cobalt(III) chloride|<nowiki>[<

==Coordination chemistry==

...avior.<ref name="Cotton1">Cotton, F.A.; Wilkinson, G. ''Advanced Inorganic Chemistry: A Comprehensive Text'', 4th ed.; Wiley-Interscience Publications: New York ...mi, G.; Rauchfuss, T.; Angelici, R. ''Synthesis and Technique in Inorganic Chemistry'', 3rd ed.; University Science Books: Sausalito, CA, 1999; pp. 85-92. ISBN

==Coordination chemistry== ...kinetically inert, allowing further synthetic transformations on the other coordination sites.

...o metal cations through the thiol groups, which ionize upon [[coordination chemistry|complexation]].

...is most often encountered as a [[tridentate]] [[ligand]] in [[coordination chemistry]]. ...9]aneS3)([9]aneS3(O))](ClO4)2.2NaClO4^.H2O | journal = Inorganic Chemistry | volume = 26 | issue = | pages = 3762–3769(8) | pmid = | doi = 10.1021/i

...s are prominent: [[2,2'-bipyridine]] is a popular ligand in [[coordination chemistry]] and [[4,4'-bipyridine]] is a precursor to the herbicide [[paraquat]]. Th ...its structure, 4,4'-bipyridine can bridge between metal centres to give [[coordination polymers]].

| Coordination = ==Coordination properties==

...Hartmut Höke "Amines, Aliphatic" in Ullmann's Encyclopedia of Industrial Chemistry, 2005 Wiley-VCH Verlag, Weinheim. DOE: 10.1002/14356007.a02 001</ref> ...an adopt several diastereomeric structures, most of which are [[Chirality (chemistry)|chiral]].

.... D.; Stiefel, E. I., Eds. “Progress in Inorganic Chemistry, Dithiolene Chemistry: Synthesis, Properties, and Applications” Wiley-Interscience: New York, 2 ...ral metal centres. Such species were originally of interest in analytical chemistry. Dithiolenes lacking benzene backbones represented an important developmen

In [[chemistry]], '''clathrochelates''' are [[ligands]] that encapsulate a metal ion. [[Ch ...ften do not directly break any metal-ligand bonds, but occur in the second coordination sphere. The slowness of the metal ion exchange allows for certain experime

...ing solvents, such as water.<ref>''Solvents and Solvent Effects in Organic Chemistry'', Christian Reichardt Wiley-VCH; 3 edition 2003 ISBN 3-527-30618-8</ref> T ...nfred Eggersdorfer “Ketones” in Ullmann’s Encyclopedia of Industrial Chemistry, Wiley-VCH, 2002, Wienheim. {{DOI|10.1002/14356007.a15_077}}</ref>

...ntate [[ligand]] in [[Inorganic Chemistry|inorganic]] and [[organometallic chemistry]]. ==Coordination chemistry==

| Coordination = ...Phenylene- and Toluenediamines” in Ullmann's Encyclopedia of Industrial Chemistry 2002, Wiley-VCH, Weinheim. {{DOI|10.1002/14356007.a19_405}}</ref>

...popularly abbreviated "diars."<ref>Holleman, A. F.; Wiberg, E. "Inorganic Chemistry" Academic Press: San Diego, 2001. ISBN 0-12-352651-5.</ref> Related, but n ==Coordination chemistry==

...the conjugate acids of [[ligand]]s that bind [[metals]] to form [[complex (chemistry)|complexes]]. The metal [[ion]] usually has a charge of 2+ or 3+. A schem ===Supramolecular chemistry===

...alt(III) Complex of Ethylenediaminedisuccinic Acid | journal = Inorganic Chemistry | volume = 7 | issue = 11 | pages = 2405–2412 | date = 1968 | d ==Coordination Chemistry==

...nd 1,2-bis(diethylphosphino)ethane | journal = [[Journal of Organometallic Chemistry|J. Organomet. Chem.]] | volume = 182 | issue = 2 | year = 1979 | pages = 20

....; Rauchfuss, T. B.; Angelici, R. J., Synthesis and Technique in Inorganic Chemistry, University Science Books: Mill Valley, CA, 1999.ISBN 0935702482</ref> ...ing iron complexes are more complex owing to variable oxidation states and coordination numbers. Well-studied derivatives include the ferric compounds, e.g. Fe(TP

...Acid and Related Chelating Agents" in Ullmann's Encyclopedia of Industrial Chemistry, Wiley-VCH, Weinheim, 2005.{{DOI|10.1002/14356007.a10_095}}</ref> ...ate base]] that is the [[ligand]], and H₄EDTA, the [[precursor (chemistry)|precursor]] to that ligand. At very low pH (very acidic conditions) the f

...stants of complexes|stability constant]] for the formation of a [[Complex (chemistry)|complex]] follows the order ...cite book|last=Orgel|first=L. E.|title=An introduction to transition-metal chemistry: ligand-field theory |publisher=Methuen|location=London|date=1966|edition=2

...(s) of the complex(es) in solution. There are many areas of application in chemistry, biology and medicine. ...50 years after [[Alfred Werner]] had proposed the correct structures for [[coordination complexes]], have been summarised by Beck and Nagypál<ref>{{cite book

...However, none of the first row elements has a monomeric oxyanion with that coordination number. Instead, [[carbonate]] (CO₃^2&minus;) and [[ni In the third and subsequent rows of the periodic table, 6-coordination is possible, but isolated octahedral oxyanions are not known because they w

where {A} is the [[activity (chemistry)|activity]] of the chemical species A, etc. (activity is a dimensionless qu In organic chemistry and biochemistry it is customary to use pK_a values for acid diss

...[[equilibrium constant]] for a chemical reaction known as [[Dissociation (chemistry)|dissociation]] in the context of [[acid-base reactions]]. The equilibrium ...values of the many acids and bases present in the cell and in the body. In chemistry, a knowledge of p''K''_a values is necessary for the preparation

...rk resulted in his sharing with [[John Kendrew]] the 1962 [[Nobel Prize in Chemistry]]. ...name="Kessel 2003">van Kessel et al. "2.4 Proteins - Natural Polyamides." Chemistry 12. Toronto: Nelson, 2003. 122. Print.</ref> Most of the amino acids in hem

[[Category:Coordination chemistry]] [[Category:Polymer chemistry]]

...ns for cationic [[metal complex]]es with an [[18-Electron rule|unsaturated coordination sphere]]. These special anions are essential components of [[Homogeneous c ...rength | year = 1989 | journal = [[Inorganic_Chemistry_(journal)|Inorganic Chemistry]] | volume = 28 | issue = 14 | pages = 2869–2886 | doi = 10.1021/ic00313a

...J. Trans-effects in octahedral transition metal complexes. ''Coordination Chemistry Reviews'' '''2000''', ''203'', 5-80.</ref> ...{{Cite book | author = [[Robert H. Crabtree]] | title = The Organometallic Chemistry of the Transition Metals | year = 2005 | edition = 4th edition | isbn = 0-4

...on metal]] compounds, all of which can be considered [[complex (chemistry)|coordination complexes]]. CFT successfully accounts for some [[magnetic]] properties, c ...splitting diagrams can aid in the prediction of the magnetic properties of coordination compounds. A compound that has unpaired electrons in its splitting diagram

*D. F. Shriver and P. W. Atkins <u>Inorganic Chemistry</u> 3rd edition, Oxford University Press, 2001. Pages: 227-236. [[Category:Inorganic chemistry]]

...ond theory]] in [[quantum chemistry]]) is a popular method in coordination chemistry to estimate the [[oxidation state]]s of atoms. ...lines of force are divided equally between the bonds to the corners of the coordination polyhedron.<br />

...etry''' is used in a number of related fields of chemistry and solid state chemistry/physics. The coordination geometry of an atom is the geometrical pattern formed by atoms around the c

...how a group of ''contiguous'' [[atom]]s of a [[ligand]] are [[coordination chemistry|coordinated]] to a central atom. Hapticity of a ligand is indicated by the The η-notation is encountered in many coordination compounds:

...single atom bridges two metals, the bridging ligand is preceded by "[[Mu (chemistry)|μ]]"<ref>{{GoldBookRef|title=µ- (mu)|url=http://goldbook.iupac.org/M0365 [[Category:Coordination chemistry]]

...ics)|absorption]]s in the UV and visible [[electromagnetic spectrum]] of [[coordination compound]]s. ...complex ions'', little was known about the excited electronic states of [[coordination complex|complex metal ions]]. They used [[Hans Bethe]]'s [[crystal field t

They are often used in transition-metal chemistry to describe the repulsion energy associated with an electronic [[term symbo [[Category:Coordination chemistry]]

'''Linkage isomerism''' is the existence of [[Complex (chemistry)|co-ordination compound]]s that have the same composition differing with th ...b>)₅(NO₂)]Cl₂. The [[cation]]ic cobalt [[Coordination complex|complex]] exists in two separable linkage isomers. In the yellow-c

In [[coordination chemistry]], '''ammine complexes''' are [[metal complex]]es containing at least one [ [[Cisplatin]] is a coordination compound containing two chlorido and two ammine ligands. It is a [[metal-ba

...but the terminology is popular in textbooks, especially those describing [[coordination compound]]s. Once such a bond has been formed, its strength and description ...a so-called ''adduct''. The process of forming a dipolar bond is called ''coordination''. The electron donor acquires a positive [[formal charge]], while the elec

In [[chemistry]] and [[crystallography]], the '''coordination number''' of a central atom in a [[molecule]] or [[crystal]] is the number .../sub>]^1- has Cr³⁺ as its central cation, which has a coordination number of 6.

'''Coordination isomerism''' is a form of [[structural isomerism]] in which the composition [[Coordination complex]]

[[Category:Coordination chemistry]]

...is called the Bailar twist in honor of John C. Bailar, Jr., an [[inorganic chemistry|inorganic chemist]] who investigated this process.<ref>{{cite journal | journal = Inorganic Chemistry

...mid. This pathway is called the Ray-Dutt twist in honor of the [[inorganic chemistry|inorganic chemist]]s who proposed this process.<ref>{{cite journal | journal = Inorganic Chemistry

...'' (3rd Edition) by Gary L. Miessler, Donald A. Tarr</ref><ref>''Inorganic Chemistry'' by D. F. Shriver, P. W. Atkins</ref>. In '''oxidative addition''', a metal complex with vacant coordination sites and a relatively low [[oxidation state]] is oxidized by the [[Inserti

...polyamine metal hydroxide:<ref>G. L. Miessler and D. A. Tarr “Inorganic Chemistry” 3rd Ed, Pearson/Prentice Hall publisher, ISBN 0-13-035471-6.</ref> [[Category:Coordination chemistry]]

==Transition metal chemistry== ...ng | author = Rob Janes and Elaine A. Moore | publisher = Royal Society of Chemistry | year = 2004 | isbn = 0854049797 | url = http://books.google.com/?id=qsP7m

...er ligand, although in some cases one arm is hemi-labile and an additional coordination site is generated transiently. Early examples of pincer ligands (not calle Many tridentate ligands types occupy three contiguous, coplanar coordination sites. The most famous such ligand is [[terpyridine]] (“terpy”). Terpy

[[Category:Organometallic chemistry]] [[Category:Coordination chemistry]]

...bol ''B'', that occurs when a transition metal free ion forms a [[complex (chemistry)|complex]] with [[ligands]]. The name comes from the [[Greek language|Greek *[[Complex (chemistry)]]

...sify [[chelation|chelating]] [[ligand]]s in inorganic and [[organometallic chemistry]]. Together with [[ligand cone angle]], this parameter is relevant to diph ...atalysis was the use of triphenylphosphine in “[[Walter Reppe|Reppe]]” chemistry (1948), which included reactions of [[alkyne]]s, [[carbon monoxide]], and [

{{about|ligands in inorganic chemistry|ligands in biochemistry|Ligand (biochemistry)|other uses|Ligand (disambigua ...also: [[functional group]]) that binds to a central metal-atom to form a [[coordination complex]]. The bonding between metal and ligand generally involves formal

...chains to link the donor functionalities, but such ligands often lead to [[coordination polymer]]s. ...in Cavity: is Transdip an Authentic Trans - Spanning Ligand? | journal = [[Chemistry: A European Journal]] | volume = 13 | pages = 9448–9461 | doi = 10.1002/c

.../D01594.html ''denticity'']</ref><ref>von Zelewsky, A. "Stereochemistry of Coordination Compounds" John Wiley: Chichester, 1995. ISBN 047195599.</ref> In many cas ...are particularly useful for binding lanthanide ions, which typically have coordination numbers greater than 6.

| Coordination = <!-- edge-shared bioctahedron --> ..."tren," it is the archetypal tripodal ligand of interest in [[coordination chemistry]].

...elements|11]] and [[group 12 elements|12]].<ref> Encyclopedia of Inorganic Chemistry, 1994, John Wiley and Sons, ISBN 0-471-93620-0</ref> Similarly, Lewis bases [[Category:Coordination chemistry]]

...L. Miessler | coauthors = Donald A. Tarr | year = 1998 | title = Inorganic Chemistry (2nd edition)| publisher = Pearson Education, Inc. Pearson Prentice Hall | ...l|''d''-orbitals]] plays an important role in the electron spin state of a coordination complex. There are three factors that affect the Δ: the period of the meta

...] complexes, but resembles the [[SN2 reaction|Sn2 mechanism]] in [[organic chemistry]]. The opposite pathway is [[dissociative substitution]], being analogous Examples of associative mechanisms are commonly found in the chemistry of 16e square planar metal complexes, e.g. [[Vaska's complex]] and [[Potass

...] complexes, but resembles the [[SN1 reaction|Sn1 mechanism]] in [[organic chemistry]]. The opposite pathway is [[associative substitution]], being analogous t ...[[nucleophile]] has no influence on this rate. An intermediate of reduced coordination number can be detected. Complexes that undergo dissociative substitution a

In chemistry and physics, '''LIESST (Light-Induced Excited Spin-State Trapping)''' is a [[Category:Coordination chemistry]]

...exed to the metal and it is the ligands that are involved in the reduction chemistry instead of the metal due to electronic destabilization by being significant ...of sterically induced reductions allows the unique reducing properties and chemistry to be applicable to all of the lanthanide metals while remaining in their m

...[[square planar molecular geometry|square planar]] or [[trigonal pyramid (chemistry)|pyramidal]] geometries. This is usually dictated by [[lone pair|lone elec [[Category:Coordination chemistry]]

...sub>(NH₃)₄]⁺ <br>The colored atoms form a coordination sphere around the ion of [[cobalt]] ]] In [[coordination chemistry]], the '''coordination sphere''' refers to a central atom or ion and an array of molecules or anio

| title = Inorganic Chemistry

In [[chemistry]], a '''coordination complex''' or '''metal complex''', is a structure consisting of a central a <ref>[http://goldbook.iupac.org/C01330.html IUPAC definition of coordination entity]</ref>

.... A. Nugent and J. M. Mayer; Wiley-Interscience, New York, 1988.</ref> [[Coordination complex]]es featuring multiply bonded ligands are of both scholarly and pra [[Category:Coordination chemistry]]

...ion]] of the [[valence electron]]s of a [[transition metal]] center in a [[coordination complex]].<ref>{{Cite journal | journal = Journal of Organometallic Chemistry

[[Category:Coordination chemistry]]

...ination chemistry, the '''oxidation number''' of a central [[atom]] in a [[coordination compound]] is the charge that it would have if all the [[ligand]]s were rem (in a coordination compound, all shared electron pairs are donated by the ligands). Imagine th

...ls.png|thumb|right|200px|Idealized structure of a compound with octahedral coordination geometry.]] ...s, is referred to as octahedral.<ref>von Zelewsky, A. "Stereochemistry of Coordination Compounds" John Wiley: Chichester, 1995. ISBN 047195599.</ref>

In chemistry, '''intervalence charge transfer''', often abbreviated '''IVCT''' or even ' ...nomenon is most often observed in [[mixed-valence]] bi- and polymetallic [[coordination complex]]es. The IVCT band is usually observed in the visible or near [[inf

...ciety, Washington, D. C.</ref> is a mechanism and rate law in coordination chemistry governing the [[associative substitution]] reactions of octahedral complexe ...n-Wilkins rate law follows:<ref>G. L. Miessler and D. A. Tarr “Inorganic Chemistry” 3rd Ed, Pearson/Prentice Hall publisher, ISBN 0-13-035471-6.</ref>

...entanuclear complex undergo SCO and that the phenomenon is affected by its coordination and solvent environment. (5) Cotton, F. A.; Wilkinson, G.; Gaus, P. L. Basic Inorganic Chemistry; 3rd ed.; Wiley, 1995.<br />

...f the central atom.<ref name = "IUPAC inorganic">NOMENCLATURE OF INORGANIC CHEMISTRY IUPAC Recommendations 2005 ed. N. G. Connelly et al. RSC Publishing | ''L''-2 ||linear - 2 coordinate||[[Linear (chemistry)]]

[[Category:Coordination chemistry]]

The biological term [[Symbiosis]] was adopted for chemistry by Jøergensen in 1964<ref>C. K. Jøergensen; ''Inorg. Chem.''; 1971, '''10 [[Category:Coordination chemistry]]

...tive energies of [[term symbol|elecronic terms]] in [[transition metal]] [[coordination complex|complexes]], much like [[Tanabe-Sugano diagram]]s. They are named a [[Category:Coordination chemistry]]

==Chemistry== Salvinorin A is not an [[alkaloid]], (meaning it does not contain a [[Base (chemistry)|basic]] [[nitrogen]]), unlike most known [[opioid receptor]] [[ligand]]s.<

| Coordination = ...butylphenyl)propionatocopper(II) |journal=Journal of Inorganic and Nuclear Chemistry|volume=43|issue=11| doi = 10.1016/0022-1902(81)80610-0}}</ref><ref name="Ab

...=15728132}}</ref> The first [[excimer laser]] design used a xenon [[Dimer (chemistry)|dimer]] molecule (Xe₂) as its [[Active laser medium|lasing medi |title=Chemistry at its Most Beautiful

| Coordination = ...' “Chlorinated Hydrocarbons” in Ullmann’s Encyclopedia of Industrial Chemistry, 2006, Wiley-VCH, Weinheim. {{DOI|10.1002/14356007.a06_233.pub2}}</ref>

Posada was born in [[Cienfuegos]], Cuba. He studied medicine and chemistry at the [[University of Havana]], and worked as a supervisor for the [[Fires |quote= After studying medicine for two years and then chemistry, Mr. Posada went to work for the Firestone Tire and Rubber Company, first i