Organometallic precursor

The decomposition of metal precursors in its zerovalent state constitutes a supplementary synthetic method to produce stable and well-dispersed NPs in ILs. As an 

This is in agreement with earlier observations on the formation of nickel NPs with a narrow size distribution from the decomposition of [Ni(cod)2] in imidazolium ILs [50, 51]. 

Metal carbonyl compounds are other suitable precursors for the synthesis of NPs by thermal decomposition. The main advantage is the formation of CO that is expelled from the IL phase due to its poor solubility. However, high temperatures are commonly used to decompose such precursors. Metal NPs of Cr(0), Mo(0), and W(0) were prepared by thermal or photolytic decomposition of their respective monometallic carbonyl compounds [M(CO)6] dispersed in ILs [52]. Similarly, the precursors [Fe2(CO)9], [Ru3(CO)i2], and [Os3(CO)12] were employed in order to obtain stable metal NPs (1.5-2.5 nm) in BMI.BF4 [53]. The same procedure was extended to the preparation of lr(0), Rh(0), and Co(0) NPs in ILs [54]. 

Transfer from an Aqueous/Organic Phase to the Ionic Liquid Phase 

The organic phase transfer was observed for surfactant-stabilized Rh(0) NPs previously synthesized in an aqueous solution of N,N-dimethyl-N-dodecyl-N-(2-hydroxyethyl)ammonium chloride (HEA12.C1) [60]. The addition of LiNTf2 to the aqueous suspension of Rh-HEA12.C1 transferred the hydrosol NPs to the IL phase (HEA12.NTf2). 

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Trentler T J ef a/1997 Solution-liquid-solid growth of indium phosphide fibers from organometallic precursors elucidation of molecular and non-molecular components of the pathway J. Am. Chem. Soc. 119 2172... 

MetallorganicMBE (MOMBE). tire solid source Knudsen cells in conventional MBE are replaced witli gaseous beams of organometallic precursors, directed toward a heated substrate in UHV. Compared to MOCVD, MOMBE eliminates gas phase reactions tliat may complicate tire deposition surface reactions, and provides lower growtli temperatures. 

At the start of this Chapter, an essay by Peter Day was quoted in which he lauds the use of soft chemistry , exemplifying this by citing the use of organometallic precursors for making thin films of various materials used in microelectronics. The same approach, but without the softness, is increasingly used to make ceramic fibres here, ceramic includes carbon (sometimes regarded as almost an independent state of matter because it is found in so many forms). 

Metal clusters on supports are typically synthesized from organometallic precursors and often from metal carbonyls, as follows (1) The precursor metal cluster may be deposited onto a support surface from solution or (2) a mononuclear metal complex may react with the support to form an adsorbed metal complex that is treated to convert it into an adsorbed metal carbonyl cluster or (3) a mononuclear metal complex precursor may react with the support in a single reaction to form a metal carbonyl cluster bonded to the support. In a subsequent synthesis step, metal carbonyl clusters on a support may be treated to remove the carbonyl ligands, because these occupy bonding positions that limit the catalytic activity. 

The field of surface-mediated synthesis of metal carbonyl clusters has developed briskly in recent years [4-6], although many organometallic chemists still seem to be unfamiliar with the methods or consider themselves ill-equipped to carry them out. In a typical synthesis, a metal salt or an organometallic precursor is brought from solution or the gas phase onto a high-area porous metal oxide, and then gas-phase reactants are brought in contact with the sample to cause conversion of the surface species into the desired products. In these syntheses, characteristics such as the acid-base properties of the support influence fhe chemisfry, much as a solvenf or coreactant influences fhe chemisfry in a convenfional synfhesis. An advanfage of... 

Two examples stand out research on ceramic precursors and research on biomaterials via so-called biomimetic approaches. I had started the systematic organometallic precursor work for making ceramic powders in a series of a few dozen papers starting in 1948 (1, 2). By the mid-1950s I had shown that inorganic sols did essentially as well and were orders of magnitude cheaper. The very sophisticated ceramic precursor work, now a decade old, has yet to demonstrate a special niche for itself in any real examples with unique properties. 

Generally, stable and well-dispersed metal NPs have been prepared in ILs by the simple reduction of the M(I-IV) complexes or thermal decomposition of the organometallic precursors in the formal zero oxidation state. Recently, other methods such as the phase transfer of preformed NPs in water or organic solvents to the IL and the bombardment of bulk metal precursors with deposition on the ILs have been reported. However, one of the greatest challenges in the NPs field is to synthesize reproducibly metal NPs with control of the size and shape. Selected studies of the preparation of metal NPs in ILs that, in some cases, provide NPs with different sizes and shapes are considered in this section. 

With the surface ionization source it is generally assumed that the reactant ion internal state distribution is characterized by the source temperature and that the majority of the reactant ions are in their ground electronic state. This contrasts with the uncertainty in reactant state distributions when transition metal ions are generated by electron impact fragmentation of volatile organometallic precursors (10) or by laser evaporation and ionization of solid metal targets (11). Many examples... 

Several other methods of generating dihalocarbenes in solution have been reported the most useful of these appears to be the thermolysis of phenyltrihalo-metkyl mercury compounds as reported by Seyferth and co-workers 3 7a although other organometallic precursors have also been employed 37b ... 

Recently, Dupont and coworkers described the use of room-temperature imi-dazolium ionic liquids for the formation and stabilization of transition-metal nanoparticles. The potential interest in the use of ionic liquids is to promote a bi-phasic organic-organic catalytic system for a recycling process. The mixture forms a two-phase system consisting of a lower phase which contains the nanocatalyst in the ionic liquid, and an upper phase which contains the organic products. Rhodium and iridium [105], platinum [73] or ruthenium [74] nanoparticles were prepared from various salts or organometallic precursors in dry 1-bu-tyl-3-methylimidazolium hexafluorophosphate (BMI PF6) ionic liquid under hydrogen pressure (4 bar) at 75 °C. Nanoparticles with a mean diameter of 2-3 nm... 

Transmission infrared spectroscopy is an important tool in catalyst preparation to study the decomposition of infrared-active catalyst precursors as a result of drying, calcination or reduction procedures. In particular, if catalysts are prepared from organometallic precursors, infrared spectroscopy is the indicated technique for investigation [26]. 

Scheme 15.3 Preparation of soluble iridium nanoparticles from in situ reduction of the organometallic precursor [ir(COD)Cl]2 in imidazolium ionic liquids.

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