Search results

...[[catalyst]]s in [[organic reaction]]s.<ref>''Synthesis of Organometallic Compounds: A Practical Guide'' Sanshiro Komiya Ed. S. Komiya, M. Hurano 1997</ref> ..."Crabtree">{{cite book | last = Crabtree | first = Robert H. | title = The Organometallic Chemistry of the Transition Metals | edition = 4th | publisher = Wiley-Inte ...

{{Short description|Chemical compounds with at least one palladium atom}} ...>2+</sup>. [[Palladium(III) compounds]] have also been reported. Palladium compounds are frequently used as catalysts in [[cross-coupling reaction]]s such as th ...

{{Short description|Series of chemical reactions by which compounds exchange ligands}} ...to [[Coordination chemistry|coordination]] and [[Organometallic chemistry|organometallic]] complexes, but resembles the [[SN1 reaction|S_N1 mechanism]] in ...

...ssue=7 |pages=2512–2514 |doi=10.1021/ja00762a056}}</ref> and is one of few compounds in which cobalt has a formal [[oxidation state]] of +4. ...last1=Bower |first1=Barton K. |title=Tetra(bicycloheptyl) transition metal compounds |url=https://patents.google.com/patent/US3705916 |date=12 December 1972}} ...

{{Short description|Organometallic chemistry rule}} ...10.1016/0040-4020(78)87001-X}}</ref> The rules were published in 1978 by organometallic chemists [[Stephen G. Davies]], [[Malcolm Green (chemist)|Malcolm Green]], ...

...olfgang A. Herrmann]], Christian Erich Zybill | title=Synthetic Methods of Organometallic and Inorganic Chemistry, Volume 4, 1997 Volume 4: Sulfur, Selenium and Tell {{potassium compounds}} ...

In [[organometallic]] chemistry, '''f-block metallocenes''' are a class of [[sandwich compound] ...he coordination, activation and transformation of a variety of unsaturated compounds, including olefins,<ref name=":3" /><ref>Evans, W. J.; Ulibarri, T. A.; Zil ...

...{cite book |last1=Macintyre |first1=Jane E. |title=Dictionary of Inorganic Compounds |date=23 July 1992 |publisher=[[CRC Press]] |isbn=978-0-412-30120-9 |page=3 ...1=Frank T. |last2=Herrmann |first2=Wolfgang A. |title=Synthetic Methods of Organometallic and Inorganic Chemistry, Volume 6, 1997: Volume 6: Lanthanides and Actinide ...

...1=Frank T. |last2=Herrmann |first2=Wolfgang A. |title=Synthetic Methods of Organometallic and Inorganic Chemistry, Volume 6, 1997: Volume 6: Lanthanides and Actinide {{Lutetium compounds}} ...

...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 ...

...d in a [[coordination complex]] is involved, these reactions are typically organometallic in nature and involve a bond between a [[transition metal]] and a [[carbon] ...= McKervey|first2 = M. A.|title = Organic Synthesis with α-Diazo Carbonyl Compounds|journal = [[Chem. Rev.]]|year = 1994|volume = 94|issue = 4|pages = 1091–116 ...

[[Curium]] (Cm) usually forms compounds in the +3 oxidation state, although compounds with curium in the +4, +5 and +6 oxidation states are also known. ...enthalpies of formation of BaCmO3 and BaCfO3|journal=Journal of Alloys and Compounds|volume=200|issue=1–2|page=181|date=1993|doi=10.1016/0925-8388(93)90491-5|ur ...

In [[organometallic chemistry]], '''metal tetranorbornyls''' are compounds with the formula M(nor)₄ (M = a metal in a +4 oxidation state) ( ...:2">{{Cite journal |title=Dispersion Effects in Stabilizing Organometallic Compounds: Tetra-1-norbornyl Derivatives of the First-Row Transition Metals as Except ...

...n Acidity scale of Tetrafluoroborate Salts of Phosphonium and Iron Hydride compounds in [D2]Dichloromethane|year=2007|volume=13|issue=13|pages=3796–3803|doi=10. ...<ref>C. A. Tolman, ''Chem. Rev.'', Steric effects of Phosphorus Ligands in Organometallic Chemistry and Homogeneous Catalysis., 1977, volume 77, pages 313-348. {{doi ...

{{short description|Chemical compounds}} .../ref><ref name=e45>Peterson, p. 45</ref> Berkelium can also form several [[organometallic compound]]s. ...

{{Short description|Methods of hydrogenation and hydrogenolysis of organic compounds}} ...carbon.<ref>{{cite journal|doi=10.1002/0471264180.or071.01|title=Ionic and Organometallic-Catalyzed Organosilane Reductions|journal=Organic Reactions|year=2008|last1 ...

...amarium(II) iodide''' involve the conversion of various classes of organic compounds into reduced products through the action of [[samarium(II) iodide]], a mild *α-Functionalized carbonyl compounds ...

...Reagent for Generation and Stabilization of Cationic, Highly Electrophilic Organometallic Complexes|journal = [[Organometallics]]|year = 1992|volume = 11|issue = 11| ==Synthesis of BARF compounds== ...

...linkinghub.elsevier.com/retrieve/pii/S0022328X00920655 |journal=Journal of Organometallic Chemistry |language=en |volume=170 |issue=3 |pages=271–284 |doi=10.1016/S00 {{Beryllium compounds}} ...

...by the low cost of ethylene as a reagent and its selectivity. It produces compounds with [[terminal alkene]] [[functional group]]s (α-olefins), which are more [[Category:Organometallic chemistry]] ...