Germanium, synthesis

Heath J R and LeGoues F K 1993 A liquid solution synthesis of single crystal germanium quantum wires Chem. Phys. Lett. 208 263... 

Heath J R, Shiang J J and Alivisatos A P 1994 Germanium quantum dots optical properties and synthesis J. Chem. Phys. 101 1607... 

Unsolvated organomagnesium compounds have been recommended for the synthesis of organometallic derivatives of mercury, boron, aluminum, silicon, germanium, tin, phosphorus, arsenic, and antimony6-8 and have been used in procedures for the alkylation of aromatic rings and for the production of various polymerization catalysts.4 9... 

Whether these results will also have an impact on the theory of metallaallenes is difficult to predict at least for the compounds Cp (CO)2Mn = M = Mn(CO)2Cp, (M = Ge, Sn, Pb) a linear structure is established and also linear p-carbido complexes are known [198], Recently, a germanium compound has been synthesized which is directly comparable with 22. In this case, the starting material for the synthesis is not a monomeric base adduct, but a dimeric germylene complex which is cleaved by Na2Fe(CO)4 in pyridine to form 72 [199],... 

The state of the synthetic art in this area, in 1979, is much more satisfactory. During the past decade, several new synthetic developments have occurred such that we are closer to the point where the limitations upon synthesis of trifluoromethyl compounds are related more to stability problems in isolated cases, and are not nearly so much due to lack of widely applicable synthetic techniques. We find ourselves, for example, in a position in 1979 where the germanium compound, Ge(CF3)4, which in the past decade, was considered by many workers to be of insufficient stability to permit isolation, has been prepared by four independent methods and is known to be stable to over 100°C. Many of these new synthetic techniques have emerged from studies conducted in our laboratory at the University of Texas and previously... 

In order to test the generality of the synthesis, the reaction of (CzFsljHg with Gel was assessed. This reaction required a higher temperature, 135°, before it proceeded measurably. (Pentafluoroethyl)ger-manium triiodide was the only (perfluoroethyl)germanium halide produced, in 54% yield (15). From this reaction, perfluoroethyl iodide was also isolated (in 30% yield). The reactions of GeBr4 with (CF3)2Hg and (C2F5)2Hg were similar in nature (16). 

Ellman JA, Plunkett MJ. Germanium and silicon linking strategies for traceless solid-phase synthesis. J Org Chem 1997 62 2885-2893. 

Although some review articles are now available on the synthesis of heavy ketones," they are restricted to dealing with some selected elements, especially silicon and germanium. We delineate here a more general account of the whole chemistry of stable double bonds between heavier Group 14 and Group 16 elements [i.e., RR M=X (M = Si, Ge, Sn, Pb X = O, S, Se, Te)]. 

Meanwhile, Parkin and his co-workers have also reportedthe synthesis of a series of terminal chalcogenido complexes of germanium 66, 67, and 68 (Scheme 20).42 X-ray structural analyses of 66, 67, and 68 revealed that they have unique germa-chalcogenourea structures stabilized by the intramolecular coordination of nitrogen atoms. The central Ge-X (X = S, Se, Te) bond of 66, 67, and 68 should be represented by a resonance structure, Ge+ - X- —>- Ge=X, because their bond... 

A variety of preparation methods are known for transient germanium-chalcogen double bond species some of them seemed to be useful also for the synthesis of kinetically stabilized systems. Indeed, the reaction of a germylene with an appropriate chalcogen source was found to be one of the most versatile and general methods for the synthesis of stable germanium-containing heavy ketones (Scheme 21). 

In view of these situations, synthesis and isolation of a kinetically stabilized germanetellone are significant not only for clarifying the character of the Ge-Te double bond by itself but also for elucidating the properties of germanium-containing heavy ketones systematically. 

Synthesis of Alkyl,aryl-Substituted Germanium-Containing Heavy Ketones... 

Aminolysis of the corresponding halides is the preferred method for the synthesis of dialkylamino derivatives of boron,1 silicon,2 germanium,3 phosphorus,4 arsenic,5 and sulfur.6 (Dialkylamino) chlorosilanes are prepared stepwise by the reaction of silicon tetrachloride with dialkylamines. This method may be utilized equally well for the conversion of alkyl- or aryl-substituted halides [e.g., (CH3) SiCl4. ] or of oxide and sulfide halides (e.g., POCl3 or PSC13) to the corresponding dialkylamino compounds. 

Al-containing ITQ-21 zeolite ((Si+Ge)/Al=25, Si/Ge=20) was synthesized using N(16)-methyl-sparteinium cation (MSPT+) as the organic structure-directing agent in combination with fluoride anions and germanium as described in [1], The composition of the final synthesis gel was ... 

Limited studies of the germanium and tin hydride analogs of the silicon hydrides show that they share this ability to function as hydride sources in ionic hydrogenations however, their relatively greater reactivity toward acids appears to restrict their practical applications in organic synthesis.24,25... 

The single-bond compounds between Si, Ge, and Sn and chalcogens (S, Se, Te) are reactive and used as synthetic intermediates in the synthesis of organic compounds, organochalcogen compounds, organo-silicon, -germanium and -tin compounds, and transition metal-chalcogen complexes and clusters. 

Mitzi, D. B. 2005. Synthesis, structure, and thermal properties of soluble hydrazinium germanium(IV) and tin(IV) selenide salts. Inorg. Chem. 44 3755-3761. 

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