Wikipedia contributions by Smokefoot

[[WP:AES|←]]Redirected page to [[Polyene]]

[[WP:AES|←]]Created page with '{{Short description|Coordination compound}} In [[organometallic chemistry]], a '''transition metal diene complex''' is a [[coordination compound]] containing one or more [[diene]]s [[ligand]]s. The inventory is large.<ref name=Elsch>Elschenbroich, C. "Organometallics" (2006) Wiley-VCH: Weinheim. {{ISBN|3-527-29390-6}}</ref> Such compounds are intermediates in many catalytic reactions that convert dienes to other organic products.<ref>{{cite book |title=Orga...'

#REDIRECT [[1,3,5-Hexatriene]]

[[WP:AES|←]]Redirected page to [[Pentadienyl]]

Add: page, volume, date, journal, title. | [[:en:WP:UCB|Use this tool]]. [[:en:WP:DBUG|Report bugs]]. | #UCB_Gadget

[[WP:AES|←]]Redirected page to [[Diene#1,3-Diene]]

[[WP:AES|←]]Redirected page to [[Transition metal sulfito complex]]

[[WP:AES|←]]Redirected page to [[Metal sulfur dioxide complex]]

[[WP:AES|←]]Redirected page to [[Transition metal sulfito complex]]

[[WP:AES|←]]Redirected page to [[O-Anisidine]]

[[WP:AES|←]]Created page with 'Pigment Yellow are [[organic pigment]]s generally derived from 3,3'-dichlorobenzidine. Several are commercially important.<ref>{{cite journal |last1=Barrow |first1=Michael J. |last2=Christie |first2=Robert M. |last3=Badcock |first3=Tracey D. |title=The crystal and molecular structure of C.I. Pigment Yellow 83, a superior performance Diarylide Yellow pigment |journal=Dyes and Pigments |date=2003 |volume=57 |issue=2 |pages=99–106 |doi=10.1016/S0143-7208(02...'

the tris deriv

[[WP:AES|←]]Redirected page to [[Poly(p-phenylene methylene)]]

[[WP:AES|←]]Created page with ''''Poly(p-phenylene methylene)''' is an [[organic polymer]] with the formula (C₆H₄CH₂)_n.<ref>{{cite book |last1=Brühne |first1=Friedrich |last2=Wright |first2=Elaine |title=Ullmann's Encyclopedia of Industrial Chemistry |chapter=Benzyl Alcohol |date=2000 |doi=10.1002/14356007.a04_001 |isbn=978-3-527-30385-4 }}</ref> In the simplest formulation, it consists of 1,4-phenylene rings linked by methylene groups. It...'

[[WP:AES|←]]Redirected page to [[Transition metal alkene complex]]

[[WP:AES|←]]Redirected page to [[Transition metal alkene complex#Dienes, trienes, and related ligands]]

[[WP:AES|←]]Redirected page to [[Spin crossover]]

[[WP:AES|←]]Redirected page to [[Transition metal complexes of thiocyanate]]

[[WP:AES|←]]Redirected page to [[Triphenylphosphine dibromide]]

[[WP:AES|←]]Redirected page to [[Triphenylphosphine dibromide]]

[[WP:AES|←]]Created page with ''''2-Bromonaphthalene''' is an [[organic compound]] with the formula C₁₀H₇Br. It is one of two [[isomer]]ic bromonaphthalenes, the other being [[1-Bromonaphthalene|1-bromonaphthalene]]. Under normal conditions, the substance is a colorless solid. ==Synthesis and reactions== It is prepared by treatment of [[2-Naphthol]] with [[bromine]]:<ref>{{cite journal | doi = 10.15227/orgsyn.049.0006| title = 2-Bromonaphthalene| journal = Organic...'

[[WP:AES|←]]Created page with '{{Short description|Class of chemical compounds}} '''Thiuram monosulfides''' are a class of [[organosulfur compound]]s with the formula (R₂NCS)₂S. Many examples are known, but popular ones include R = [[methyl|Me]] and R = [[Ethyl group|Et]]. They are typically white or pale yellow solids that are soluble in organic solvents.<ref name=Ullmann>{{cite book |last1=Schubart |first1=Rüdiger |title=Ullmann's Encyclopedia of Industrial Chem...'

[[WP:AES|←]]Redirected page to [[Transition metal complexes of carbon disulfide]]

[[WP:AES|←]]Redirected page to [[Transition metal complexes of carbon disulfide]]

[[WP:AES|←]]Redirected page to [[Transition metal thiocarbonyl complex]]

[[WP:AES|←]]Created page with ''''Transition metal complexes of carbon disulfide''' are [[coordination complex]]es containing [[carbon disulfide]] as a ligand. Carbon disulfide is a well established [[commodity chemical]] with extensive reactivity, so it is logical that its interactions with metal complexes has been investigated. In terms of ligand properties, carbon disulfide is nonbasic: it has no [[Lewis base|Lewis basicity]]. It is weakly electrophilic as shown by its reduction an...'

[[WP:AES|←]]Redirected page to [[Chlorocarbonylsulfenyl chloride]]

[[WP:AES|←]]Redirected page to [[Chlorocarbonylsulfenyl chloride]]

#REDIRECT [[Phytoremediation#Phytodegradation]]

[[WP:AES|←]]Redirected page to [[Abandoned mine#Reclamation and reuse]]

[[WP:AES|←]]Redirected page to [[Polycyclic aromatic hydrocarbon]]

[[WP:AES|←]]Redirected page to [[Transition metal tetraperoxide complexes]]

[[WP:AES|←]]Redirected page to [[Transition metal pyridine complexes]]

Transition metal complexes of pyridine-N-oxides and amine oxides

[[WP:AES|←]]Redirected page to [[Hyperaccumulator]]

[[WP:AES|←]]Redirected page to [[Hyperaccumulator]]

[[WP:AES|←]]Created page with '{{Chembox | ImageFile = | ImageSize = | ImageAlt = | IUPACName = | OtherNames = cis-Diiododiammineplatinum, cis-Platinumdiammine diiodide |Section1={{Chembox Identifiers | CASNo = 15978-93-5 | CASNo_Comment = | CASNo1 = | CASNo1_Comment = | PubChem = | SMILES = }} |Section2={{Chembox Properties | Formula = | MolarMass = | RefractIndex = | Appearance = | Density = | MeltingPt = | MeltingPt_notes = | BoilingPt = | BoilingPt_notes = | Solubility =...'

[[WP:AES|←]]Redirected page to [[Triphenylstibine]]

start the spin-off of Organoantimony-based Lewis acids

[[WP:AES|←]]Created page with '{{Chembox | ImageFile = 1-Chloroanthraquinone.svg | ImageSize = | ImageAlt = | IUPACName = | OtherNames = |Section1={{Chembox Identifiers | CASNo = | CASNo_Comment = | CASNo1 = | CASNo1_Comment = | PubChem = | SMILES = }} |Section2={{Chembox Properties | C = 14|H=8|O=5|S=1 | MolarMass = | RefractIndex = | Appearance = white solid | Density = | MeltingPtC = | MeltingPt_notes = | BoilingPt = | BoilingPt_notes = | Solubility = }} |Section3={{Chembox...'

[[WP:AES|←]]Created page with '{{Chembox | ImageFile = 1-ChloroanthraquinoneNew.svg | ImageSize = | ImageAlt = | IUPACName = | OtherNames = a-chloroanthraquinone |Section1={{Chembox Identifiers | CASNo = 82-44-0 | CASNo_Comment = | CASNo1 = | CASNo1_Comment = | PubChem = 8553 | SMILES = }} |Section2={{Chembox Properties | C = 14|H=7|O=2|Cl=1 | MolarMass = | RefractIndex = | Appearance = white solid | Density = | MeltingPtC = 162 | MeltingPt_notes = | BoilingPt = | BoilingPt_note...'

[[WP:AES|←]]Created page with 'In [[organic chemistry]], the '''Fischer reaction''' is the conversion of an [[aryl sulfonic acid]] to an [[aryl chloride]] using [[chlorine]]:<ref>{{cite book |doi=10.1002/14356007.a02_355 |chapter=Anthraquinone Dyes and Intermediates |title=Ullmann's Encyclopedia of Industrial Chemistry |year=2000 |last1=Bien |first1=Hans-Samuel |last2=Stawitz |first2=Josef |last3=Wunderlich |first3=Klaus |isbn=3527306730 }}</ref> :{{chem2|ArSO3H + Cl2 -> ArCl + ClSO3H...'

[[WP:AES|←]]Created page with '{{Chembox | ImageFile = 2-ChloroanthraquinoneNew.svg | ImageSize = | ImageAlt = | IUPACName = | OtherNames = |Section1={{Chembox Identifiers | CASNo = 17-79-3 | CASNo_Comment = | CASNo1 = | CASNo1_Comment = | PubChem = 8341 | SMILES = }} |Section2={{Chembox Properties | C = 14|H=9|O=2|N=1 | MolarMass = | RefractIndex = | Appearance = white solid | Density = | MeltingPtC = 302–303 | MeltingPt_notes = | BoilingPt = | BoilingPt_notes = | Solubilit...'

[[WP:AES|←]]Created page with '{{Chembox | ImageFile = | ImageSize = | ImageAlt = | IUPACName = | OtherNames = |Section1={{Chembox Identifiers | CASNo = 131-09-9 | CASNo_Comment = | CASNo1 = | CASNo1_Comment = | PubChem = | SMILES = }} |Section2={{Chembox Properties | C = 14|H=7|O=2|Cl=1 | MolarMass = | RefractIndex = | Appearance = white solid | Density = | MeltingPtC = 210 | MeltingPt_notes = | BoilingPt = | BoilingPt_notes = | Solubility = }} |Section3={{Chembox Hazards |...'

[[WP:AES|←]]Redirected page to [[2,6-Dimethyl-2-heptanol]]

more regurgitation from Ullmann

[[WP:AES|←]]Created page with '{{Chembox | ImageFile = | ImageSize = | ImageAlt = | IUPACName = | OtherNames = Dimetol |Section1={{Chembox Identifiers | CASNo = 13254-34-7 | CASNo_Comment = | CASNo1 = | CASNo1_Comment = | PubChem = | SMILES = }} |Section2={{Chembox Properties | C=9|H=20|O =1 | MolarMass = | RefractIndex =1.4248 | Appearance = colorless liquid | Density = 0.8186 g/cm³ | MeltingPt = | MeltingPt_notes = | BoilingPtC = 170–172 | BoilingPt_notes = 101.3...'

[[WP:AES|←]]Created page with '{{Chembox | ImageFile = | ImageSize = | ImageAlt = | IUPACName = | OtherNames = 2,5-Dihydro-4-hydroxy-2-methyl-5-oxo-2-furancarboxylic acid, 4-hy­droxy-2-methyl-5-oxo-2,5-di­hydro­furan-2-carb­oxy­lic acid |Section1={{Chembox Identifiers | CASNo = 24891-71-2 | CASNo_Comment = | CASNo1 = | CASNo1_Comment = | PubChem = 71436380 | SMILES = }} |Section2={{Chembox Properties | C=6|H=6|O=5| | MolarMass = | RefractIndex = | Appearance = white solid |...'

>2900 cites

>1800 refs in CAS

[[WP:AES|←]]Redirected page to [[Radioactive waste]]

[[WP:AES|←]]Redirected page to [[Episulfide#Reactions]]

[[WP:AES|←]]Created page with '{{Chembox | ImageFile = | ImageSize = | ImageAlt = | IUPACName = | OtherNames = |Section1={{Chembox Identifiers | CASNo = 1662-01-7 | CASNo_Comment = | CASNo1 = | CASNo1_Comment = | PubChem = | SMILES = }} |Section2={{Chembox Properties | C=24|H=16|N=2| | MolarMass = | RefractIndex = | Appearance = white solid | Density = | MeltingPtC = 180 | MeltingPt_notes = | BoilingPt = | BoilingPt_notes = | Solubility = }} |Section3={{Chembox Hazards | Mai...'

[[WP:AES|←]]Created page with '{{Chembox | ImageFile = | ImageSize = | ImageAlt = | IUPACName = | OtherNames = 1,4-Naphthoquinol |Section1={{Chembox Identifiers | CASNo = 571-60-8 | CASNo_Comment = | CASNo1 = | CASNo1_Comment = | PubChem = | SMILES = }} |Section2={{Chembox Properties | C = 10|H=8|O=2 | MolarMass = | RefractIndex = | Appearance = white solid | Density = | MeltingPtC = 190 | MeltingPt_notes = | BoilingPt = | BoilingPt_notes = | Solubility = }} |Section3={{Chembo...'

[[WP:AES|←]]Created page with '{{Chembox | ImageFile = | ImageSize = | ImageAlt = | IUPACName = | OtherNames = naphthoresorcinol |Section1={{Chembox Identifiers | CASNo = 132-86-5 | CASNo_Comment = | CASNo1 = | CASNo1_Comment = | PubChem = | SMILES = }} |Section2={{Chembox Properties | C = 10|H=8|O=2 | MolarMass = | RefractIndex = | Appearance = colorless or white solid | Density = | MeltingPtC = 122–124 | MeltingPt_notes = | BoilingPt = | BoilingPt_notes = | Solubility = }}...'

[[WP:AES|←]]Created page with ''''Naphthalenedisulfonic acid''' refers to [[organic compound]]s with the formula {{chem2|C10H6(SO3H)2}}. Some are precursors to [[azo dye]]s and to various drugs.<ref>{{cite book |last1=Booth |first1=Gerald |title=Ullmann's Encyclopedia of Industrial Chemistry |chapter=Naphthalene Derivatives |date=2000 |doi=10.1002/14356007.a17_009 |isbn=978-3-527-30385-4 }}</ref> They are colorless solids with high solubility in water. {| class="wikitable" |+ Hydroxy...'

[[WP:AES|←]]Redirected page to [[Armstrong's acid]]

[[WP:AES|←]]Redirected page to [[Peri-naphthalenes]]

[[WP:AES|←]]Created page with ''''Hydroxynaphthalenesulfonic acid''' refers to [[organic compound]]s with the formula {{chem2|C10H6(SO3H)(OH)}}. Several are precursors to [[azo dye]]s and to various [[aminonaphthalenesulfonic acid]]s.<ref>{{cite book |last1=Booth |first1=Gerald |title=Ullmann's Encyclopedia of Industrial Chemistry |chapter=Naphthalene Derivatives |date=2000 |doi=10.1002/14356007.a17_009 |isbn=978-3-527-30385-4 }}</ref> They are colorless solids with high solubility i...'

[[WP:AES|←]]Created page with '{{Chembox | ImageFile = | ImageSize = | ImageAlt = | IUPACName = | OtherNames = |Section1={{Chembox Identifiers | CASNo = 581-43-1 | CASNo_Comment = | CASNo1 = | CASNo1_Comment = | PubChem = | SMILES = }} |Section2={{Chembox Properties | C = 10|H=8|O=2 | MolarMass = | RefractIndex = | Appearance = white solid | Density = | MeltingPtC = 220 | MeltingPt_notes = | BoilingPt = | BoilingPt_notes = | Solubility = }} |Section3={{Chembox Hazards | MainH...'

[[WP:AES|←]]Redirected page to [[Cis-1,2-Dihydrocatechol]]

[[WP:AES|←]]Created page with ''''Dinitronaphthalene''' refers to [[organic compound]]s with the formula {{chem2|C10H6(NO2)2}}.<ref>{{Ullmann |doi=10.1002/14356007.a17_411|title=Nitro Compounds, Aromatic |year=2000 |last1=Booth |first1=Gerald |isbn=3527306730 }}</ref> Two isomers of dinitronaphthalene are of some commercial importance. These colorless or pale yellow solids are produced by [[nitration]] of naphthalene: * 1,6-Dinitronaphthalene ([[registry number|RN]] 605-71-0), meltin...'

[[WP:AES|←]]Redirected page to [[2-Hydroxyethyl methyl terephthalate]]

[[WP:AES|←]]Created page with ''''2-Hydroxyethyl methyl terephthalate''' is an [[organic compound]] with the formula {{chem2|HOCH2CH2O2CC6H4CO2CH3}}. It is a mixed [[ester]] of [[teraphthalic acid]]. This compound is an intermediate in the industrial production of [[polyethylene terephthalate]] (>80 Mtons/y) by the [[transesterification]] from [[dimethylterephthalate]]: :{{chem2|CH3O2CC6H4CO2CH3 + HOCH2CH2OH -> HOCH2CH2O2CC6H4CO2CH3 + CH3OH}} :{{chem2|n HOCH2CH2O2CC6H4CO2CH3 ->...'

[[WP:AES|←]]Created page with ''''Transition metal tetraperoxide complexes''' are [[coordination complex]]es with the formula {{chem2|[M(O2)4](n-)}}. They feature 8-coordinate metal centers with four side-bonded peroxide ligands. ==Titanium triad== Titanium-peroxide complexes have long been the basis of a [[colorimetric test]] for [[peroxide]].<ref>{{cite journal |last1=Hossain |first1=Rayhan |last2=Dickinson |first2=Jimmy J. |last3=Apblett |first3=Allen |last4=Materer |first4=Nicholas...'

[[WP:AES|←]]Redirected page to [[Iron(II) glycinate]]

[[WP:AES|←]]Redirected page to [[Zinc glycinate]]

[[WP:AES|←]]Redirected page to [[Iron(II) glycinate]]

[[WP:AES|←]]Redirected page to [[Zinc glycinate]]

[[WP:AES|←]]Redirected page to [[Zinc glycinate]]

[[WP:AES|←]]Created page with ' {{Chembox | ImageFile = | ImageSize = | ImageAlt = | IUPACName = | OtherNames = zinc bis(glycinate) monohydrate |Section1={{Chembox Identifiers | CASNo = 14281-83-5 | CASNo_Comment = | CASNo1 = | CASNo1_Comment = | PubChem = | SMILES = }} |Section2={{Chembox Properties | C = 4|O=5|H=6|N=2|Zn=1 | MolarMass = | RefractIndex = | Appearance = white solid | Density = | MeltingPt = | MeltingPt_notes = | BoilingPt = | BoilingPt_notes = | Solubility =...'

[[WP:AES|←]]Created page with ''''Nickel glycinate''' can refer to several nickel(II) (that is Ni²⁺) derivatives of [[glycinate]] ({{chem2|H2NCH2CO2-}}). These species are [[coordination complex]]es where glycinate functions as a bidentate ligand. More specifically, these species are a subset of [[transition metal complexes]] of amino acids. Representative examples are {{chem2|[Ni(H2NCH2CO2)2(H2O)2}}<ref>{{cite journal |last1=Freeman |first1=H. C. |last2=Guss |first2=J. M....'

[[WP:AES|←]]Redirected page to [[Tris(glycinato)cobalt(III)#Other cobalt glycinates]]

[[WP:AES|←]]Redirected page to [[Hydrogen bond]]

[[WP:AES|←]]Redirected page to [[Anion complex]]

#REDIRECT [[Anion complex]]

[[WP:AES|←]]Redirected page to [[Anion complex]]

[[WP:AES|←]]Redirected page to [[Anion complex]]

start an article

[[WP:AES|←]]Redirected page to [[Diphenyl sulfide]]

going to build this article today, parking content

[[WP:AES|←]]Redirected page to [[Phosphorus pentasulfide#Thionations]]

[[WP:AES|←]]Redirected page to [[Methyltrichlorosilane]]

[[WP:AES|←]]Redirected page to [[Nonoxynols]]

[[WP:AES|←]]Redirected page to [[Α-Olefin sulfonate]]

[[WP:AES|←]]Redirected page to [[Fatty alcohol#Applications]]

[[WP:AES|←]]Redirected page to [[Fatty alcohol#Applications]]

[[WP:AES|←]]Redirected page to [[4-Methylacetophenone]]

[[WP:AES|←]]Redirected page to [[4-Vinyltoluene]]

14000 cites

[[WP:AES|←]]Created page with '{{Chembox | ImageFile = | ImageSize = | ImageAlt = | IUPACName = | OtherNames = octahydroindene, hexahydroindane, bicyclo[4.3.0]nonane |Section1={{Chembox Identifiers | CASNo = 496-10-6 | CASNo_Comment = | CASNo1 = | CASNo1_Comment = | PubChem = | SMILES = }} |Section2={{Chembox Properties | C=9|H=16 | MolarMass = | RefractIndex = | Appearance = | Density = 0.90732 g/cm³ | MeltingPtC = -53 | MeltingPt_notes = | BoilingPtC = 165.5-167.5...'

[[WP:AES|←]]Redirected page to [[Aromatic sulfonation#Alkaline fusion]]

[[WP:AES|←]]Created page with ''''Indanol''' refers to [[hydroxy]] derivatives of [[indane]] (also known as indan). Five [[isomer]]s are possible, two of which are [[phenol]]s (4- and 5-indanols). Three isomers feature hydroxyl group on the five-membered ring, including an [[enantiomer]]ic pair of 1-indanol. 1-Indanol can be produced by reduction of [[1-Indanone|1-indanone]]. 5-indanol can be prepared by [[sulfonation]] of indane, following by base cleavage of the indane-5-sulfonate.<...'

[[WP:AES|←]]Redirected page to [[1,3-Indandione]]

[[WP:AES|←]]Redirected page to [[Malonyl chloride]]

[[WP:AES|←]]Created page with '{{Chembox | ImageFile = Ph3COOH.svg | ImageSize = 110px | ImageAlt = | IUPACName = | OtherNames = Trityl hydroperoxide |Section1={{Chembox Identifiers | CASNo = 4198-93-0 | CASNo_Comment = | CASNo1 = | CASNo1_Comment = | PubChem = | SMILES = }} |Section2={{Chembox Properties | C=19|H=16|O=2 | MolarMass = | RefractIndex = | Appearance = | Density = 1.27 g/ mL | MeltingPtC = 87.5–88.5 | MeltingPt_notes = | BoilingPt = | BoilingPt_notes = | Solubil...'

[[WP:AES|←]]Created page with '{{Chembox | ImageFile = | ImageSize = | ImageAlt = | IUPACName = | OtherNames = 2-ethylhexanoic acid, potassium salt |Section1={{Chembox Identifiers | CASNo = 3164-85-0 | CASNo_Comment = | CASNo1 = | CASNo1_Comment = | PubChem = | SMILES = }} |Section2={{Chembox Properties | C=8|H=15|O=2|K=1 | MolarMass = | RefractIndex = | Appearance = white solid | Density = | MeltingPt = | MeltingPt_notes = | BoilingPt = | BoilingPt_notes = | Solubility = }}...'

[[WP:AES|←]]Created page with 'Many gold art and artefacts have attracted attention over the course of [[human history]]. <gallery mode="packed" heights="170px"> Gold leaf MET DP260372.jpg|[[Minoan civilization|Minoan]] jewelry, 2300–2100 BC, gold, [[Metropolitan Museum of Art]], New York Blessington lunula.BM.WG.31.jpg|[[Gold lunula]], Irish, 2400{{ndash}}2000 BC [[British Museum]] Earrings from Shulgi.JPG|[[Sumer]]ian earrings with [[cuneiform]] inscriptions, 2093–2046 BC, gold, [...'

[[WP:AES|←]]Redirected page to [[Hydroxymethylation#Related reactions]]

[[WP:AES|←]]Redirected page to [[Hydroxymethylation]]

/* Preparation */ replace guessed prep (maybe ok?) with standard one

/* Preparation */ structure

/* Preparation */ structure

/* Crystal structure */ melting

/* Reactions */ moving bits

melts

/* Structure */ melting behavior

layout and mention NaSH

lede

/* Inorganic cases */ NH4Cl

KCN

/* Structure */ ref

repair box

expand structure, polymorph

swap unit cell out of chembox to text, describe its chem, rm licorice as a lede-deserving characterization

/* Production */ simplify caption (its not a synthesis)

/* Applications */ rm [[Image:Ammoniumchloride crystal 01.jpg|thumb|left|Ammonium chloride crystal(s)]]. we already have a pic

Undid revision [[Special:Diff/1357831635|1357831635]] by [[Special:Contributions/Cicognac|Cicognac]] ([[User talk:Cicognac|talk]]) spamming

[[WP:SECONDARY]]

/* Hydrates */ hierarchy

/* Chemistry */ expand

rephrase throughout

/* Carbon */ move qd's

/* Ferrous materials */ Fe

/* History */ rm header

rm [[Category:Arab inventions]] [[Category:Egyptian inventions]] [[Category:German inventions]] [[Category:Swiss inventions]]

reinstate CQD

we dont need six contemporaneous refs to a small topic

replace esoteric (nano carbon) with something macroscopic and relevant to the public

/* Safety */ lsl

/* Lead poisoning incidents */ fmt

/* Lead poisoning incidents */ chop out newspaper like reports and some scare stories with technical perspective

simplify claim

- }

/* Synthesis */ geometry

and more refs

XRD ref

expand with emphasis on inorganic aspects

replace image, might need to switch around depending on the literature. The structure of the hydrate is known.

invented (RS) topic for homework

#REDIRECT [[Degradation]]

made homework project into redirect

/* Hydrogen storage */ rephrase moribund theme

/* Inorganic chemistry */rephrase to indicate that it has been used but is not so central

/* Dienes */ cite

/* Future and aspirational themes */ ==

<ref name=UllmannCu>{{cite book |last1=Lossin |first1=Adalbert |title=Ullmann's Encyclopedia of Industrial Chemistry |chapter=Copper |date=2001 |doi=10.1002/14356007.a07_471 |isbn=978-3-527-30385-4 }}</ref>

<ref name=Ullmann>

/* History */ relocation of Cu biomining

/* Copper ores */ moving history

ref A moved

typos

rebalance eq's

genera

not oil spills

/* Biomining in space */ fmt

finish merge. Still much duplication

oop

redirect

/* Bioleaching technologies */ paste

/* Direct vs indirect leaching */ move

/* See also */ Further reading

/* Further reading */ move

rm most mentions of biohydrometallurgy

/* Environmental impact */ merging

/* Applications */ fewer sections

/* See also */ new section from merge

/* Environmental impact */ move

/* With fungi */ rm dup header

/* Biomining in space */ much duplicate material still

/* Biomining in space */ pastein

/* Fungi in biomining */ sloppy paste, temp

/* Related speculative concepts */ merging stepwise

/* Pyrite */ oop

/* Applications */ merging content from [[biohydrometallurgy]]

/* Applications */ starting the merge

[[WP:AES|←]]Redirected page to [[Polyene]]

ref

prep

/* Dienes */ link

center

/* Trienes and tetraenes */ center

ref

/* Trienes and tetraenes */ [[bis(benzene)chromium]]

/* Trienes and tetraenes */ arenes

electron count

/* Reactions and applications */ clarity

/* Bonding */ hapticity

/* Safety */ rm questionable claim

/* Dienes */ replace one image

/* Bonding */ layout

/* Bonding */ | Add: pages, issue, volume, date, journal, title, authors 1-4. | [[:en:WP:UCB|Use this tool]]. [[:en:WP:DBUG|Report bugs]]. | #UCB_Gadget

/* Bonding */ two chemdraws

red link repair

/* Reactions and applications */ allyl

/* Reactions and applications */ expand

A large number of complexes are known of the type [[(diene)iron tricarbonyl]].

/* Bonding */ repair

/* Reactions and applications */ rm Wacker scheme

split gallery