Main group metals in organic synthesis / by Yamamoto, Hisashi, Oshima, Koichiro, 1947-

Subjects: “…Organometallic compounds…”

Metal mediated template synthesis of ligands / by 485443 Costisor, Otilia, Linert, W.

Subjects: “…Organometallic compounds…”

Palladium-catalysed desulfinative cross-coupling reactions: Leveraging mechanistic insights for reaction optimisation by De Gombert, A

Subjects: “…Organometallic chemistry…”

N-heterocyclic carbene stabilisation of low valent metal centres for the activation of E-H bonds by Phillips, NA

Subjects: “…Organometallic Chemistry…”

Synthesis and reactions of titanium-nitrogen multiple bonds by Groom, L, Laura Groom

Subjects: “…Organometallic Chemistry…”

Group 4 amidinate complexes as olefin polymerisation catalysts by Scott, R

Subjects: “…Organometallic Chemistry…”

η8-Permethylpentalene Titanium Chemistry by Cooper, RT

Subjects: “…Organometallic Chemistry…”

Metal-organic frameworks : design and application / by MacGillivray, Leonard

Subjects: “…Supramolecular organometallic chemistry…”

Metal organic frameworks as heterogeneous catalysts / by Llabrš i. Xamena, Francesc X, Gascon, Jorge

Subjects: “…Supramolecular organometallic chemistry…”

Systematic nomenclature of organic, organometallic and coordination chemistry : chemical-abstracts guidelines with IUPAC recommendations and many trivial names / by 399670 Bunzli-Trepp, Ursula

Organometallic and coordination clusters and polymers : syntheses and applications : London, Ontario, Canada, May 29-June 1, 2004 / by Organometallic and Coordination Clusters and Polymers: Syntheses And Applications Symposium ( 2004 : London, Ontario, Canada), Abd-El-Aziz, Alaa S., Harvey, Pierre Dominique, 1960-

Subjects:

CORROSION RESISTANCE OF ORGANOMETALLIC COATING APLICATED IN FUEL TANKS USING ELECTROCHEMICAL IMPEDANCE SPECTROSCOPY IN BIOFUEL – PART I by Milene Adriane Luciano, Maria das Mercês Reis de Castro, Vanessa de Freitas Cunha Lins

Subjects: “…Organometallic coating; Steel fuel tanks; Electrochemical impedance spectroscopy; Resistive medium.…”
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Synthesis of Unsymmetrical Ketones Using Chelation-Controlled Sequential Substitution of N‑Triazinylamide/Weinreb Amide by Organometallic Reagents by Shotaro Hirao, Rumi Saeki, Toru Takahashi, Kento Iwai, Nagatoshi Nishiwaki, Yasushi Ohga

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Flow chemistry as green technology for the genesis and use of organometallic reagents in the synthesis of key building blocks and APIs – An update by Philipp Natho, Renzo Luisi

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Chemical approaches to organometallic chemical vapor deposition of wide band-gap II-VI layers and naonocrystal composites by Danek, Michal

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Muon-spin spectroscopy of the organometallic spin-1/2 kagome-lattice compound Cu(1,3-benzenedicarboxylate) by Marcipar, Lital, Ofer, Oren, Keren, Amit, Nytko, Emily A., Nocera, Daniel G., Lee, Young S., Helton, Joel S., Bains, Chris

“…Using muon-spin resonance, we examine the organometallic hybrid compound Cu(1,3-benzenedicarboxylate) [Cu(1,3-bdc)], which has structurally perfect spin-1/2 copper kagome planes separated by pure organic linkers. …”
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Development and applications of enantioselective organometallic catalysts : I. Organotin catalysts; and, II. Planar-chiral nitrogen heterocyclic catalysts by Liang, Jack S. (Jack Shih-Chieh), 1972-

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Solid-State Organometallic Chemistry (SMOM): synthesis, alkane dehydrogenation and surface modification of crystalline σ-alkane complexes by Bukvic, AJ

“…These are synthesised by the hydrogenation of precursor alkene or diene complexes in solid/gas single-crystal to single-crystal (SC-SC) transformations, using the Solid-State Molecular OrganoMetallic (SMOM) methodology developed by the Weller group.…”

Acyclic 1,2-dimagnesioethanes/-ethene derived from magnesium(i) compounds: multipurpose reagents for organometallic synthesis by Dange, D, Gair, A, Jones, D, Juckel, M, Aldridge, S, Jones, C

Solid–state molecular organometallic chemistry. Single–crystal to single–crystal reactivity and catalysis with light hydrocarbon substrates by Chadwick, F, McKay, A, Martinez-Martinez, A, Rees, N, Kraemer, T, Macgregor, S, Weller, A

“…[Rh(Cy2PCH2CH2PCy2)(–NBA)][BArF4] and the polymorphs of [Rh(Cy2PCH2CH2PCy2)(ethene)2][BArF4] are shown to be effective in Solid-state Molecular OrganoMetallic catalysis (SMOM–cat) for the isomerization of 1–butene to a mixture of cis– and trans–2–butene at 298 K and 1 atm, and studies suggest that catalysis is likely dominated by surface–active species. …”