Search results

...rogenation of double bonds. In this regard, it unusually tolerates sulfur compounds, which poison [[noble metal]] catalysts.<ref name=":0" /> In air, the sulfide oxidizes to [[sulfur dioxide]]: ...

...s. As an example, [[Sulfur|elemental sulfur]] reacts explosively to form [[sulfur hexafluoride]] even at −180&nbsp;°C.<ref name="Holleman"/> {{Oxygen compounds}} ...

...enter|single carbon]], hemithioacetals are [[chiral]]. A related family of compounds are the '''dithiohemiacetals''', with the formula {{chem2|R\sCH(\sSH)\sSR’} ...rst2=B. J.|last3=Bellas|first3=Michael|title=Biologically oriented organic sulfur chemistry. II. Formation of hemimercaptals or hemimercaptoles (.alpha.-hydr ...

...ef name='Perry'>Dale L. Perry, Sidney L. Phillips: ''Handbook of inorganic compounds''. CRC Press, 1995, {{ISBN|978-0-8493-8671-8}}, S. 336 ({{Google books|0fT Rubidium sulfide reacts with [[sulfur]] in [[hydrogen gas]] to form [[rubidium pentasulfide]], Rb₂S<su ...

...ethods of Organometallic and Inorganic Chemistry, Volume 4, 1997 Volume 4: Sulfur, Selenium and Tellurium | publisher=Georg Thieme Verlag | isbn=978-3-13-179 {{potassium compounds}} ...

Just like [[tetrabutyllead]], tetraphenyllead and [[sulfur]] react explosively at 150&nbsp;°C and produce [[diphenyl sulfide]] and [[l ....<ref name="Richard W. Weiss">{{cite book| author=Richard W. Weiss | title=Compounds of Germanium, Tin, and Lead, including Biological Activity and Commercial A ...

...aminosulfuranes''' is a chemical reaction that transforms oxidized organic compounds into [[organofluorine compound]]s. Aminosulfuranes selectively exchange hyd ...the reagent most commonly used to accomplish this transformation. However, sulfur tetrafluoride only reacts with the most acidic hydroxyl groups (its substra ...

The '''oxalatonickelates''' are a class of [[Chemical compound|compounds]] that contain [[nickel]] [[Coordination complex|complexed]] by [[oxalate]] ...t1=J.T.|last2=Baker|first2=W.A.|title=Nickel(II) complexes with oxygen and sulfur donors|journal=Inorganica Chimica Acta|date=January 1969|volume=3|pages=463 ...

...ch compound are not needed. It can improve the response of the FID to many compounds with poor or low response, including [[carbon monoxide]] (CO), [[carbon dio ...ide to methane, and the [[Catalyst poisoning|catalysts are poisoned]] by [[sulfur]] and [[ethylene]] among others. ...

...strate. The method is used in the [[organic synthesis|synthesis of organic compounds]].<ref name=Ullmann>{{Ullmann|doi=10.1002/14356007.a02_001|title=Amines, Al ...s, and [[amine]]s. Two new bonds form: C-H and C-X (X = carbon, nitrogen, sulfur, phosphorus, etc): ...

...f hydrogen]] with [[chalcogen]] atoms (elements of group 16: [[oxygen]], [[sulfur]], [[selenium]], [[tellurium]], [[polonium]], and [[livermorium]]). [[Water | [[hydrogen sulfide]]<br>sulfur hydride<br>(sulfane) || [[hydrosulfuric acid]] || {{chem2|H2S}} || [[Image: ...

...ome rhenium and technetium dichalcogenides|journal = Journal of Alloys and Compounds| volume = 241| pages = 34–39| year = 1996| last1 = Lamfers| first1 = H.-F.| '''Rhenium disulfide''' is an [[inorganic compound]] of [[rhenium]] and [[sulfur]] with the formula ReS₂. It has a layered structure where atoms ...

...8240}}</ref> However, modern computational techniques indicate many stable compounds have a greater charge distribution than the principle predicts (they contai ...0.5. It seemed reasonable to him that since CsF is the most ionic of ionic compounds, most, if not all substances will have atoms with even smaller charges.<ref ...

:Ba[[Sulfur|S]] + 2{{hsp}}CH₃COOH → (CH₃COO)₂Ba + [[Hy {{Barium compounds}} ...

...[[catalyst]]s in [[organic reaction]]s.<ref>''Synthesis of Organometallic Compounds: A Practical Guide'' Sanshiro Komiya Ed. S. Komiya, M. Hurano 1997</ref> Stable organorhodium compounds and transient organorhodium intermediates are used as catalyst such as in o ...

...a key component in biological degradation of halogenated aromatic organic compounds.<ref name=":3">{{Cite journal|last1=Kaschabek|first1=S. R.|last2=Reineke|fi ...s'' is its ability to utilize [[Iron–sulfur cluster|FeS clusters]] and the sulfur anion, [[tetrathionate]] (O₆S₄^2-).<ref nam ...

...([[Mercury (element)|mercury]], [[phosphorus]], [[sulfur]]) and inorganic compounds.<ref>{{Cite web|url=https://web.lemoyne.edu/giunta/classicalcs/dumas.html|t ...

...nickel is octahedrally coordinated by four sulfurs and two nitrogens. The sulfur end of the SCN⁻ ligand is doubly [[Bridging ligand|bridging]].<r {{Nickel compounds}} ...

...vier|isbn=978-1-4831-5611-8|language=en}}</ref> methods for cleaving the [[sulfur]]–carbon bonds of sulfones are typically reductive in nature. Olefination o ...ne of the sulfur-carbon bonds of the sulfonyl group is cleaved, leading to sulfur-free organic products. Depending on the nature of the substrate and reactio ...

...(GAC), often used as to treat both liquid and gas phase [[volatile organic compounds]] and [[organic compound|organic]] pollutants.<ref>{{Cite journal | title = Oxidative removal of malodorous volatile sulfur compounds by air over an activated carbon fiber ...