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Formation spectroscopy

Al-Obaidi A H R, Rigby S J, Hegarty J N M, Bell S E J and McGarvey J J 1996 Direct formation of silver and gold metal liquid-like films (MELLFS) from thiols and sols without organic solvents SERS and AFM studies ICORS 96 XVth Int. Conf on Raman Spectroscopy ed S A Asher and P B Stein (New York Wiley) pp 590-1... [Pg.1232]

Hasegawa Y and Avouris Ph 1993 Direct observation of standing wave formation at surface steps using scanning tunnelling spectroscopy Rhys. Rev. Lett. 71 1071... [Pg.1721]

Besides the MDL Molfile formal, other file formats are often used in chemistry SMILES has already been mentioned in Section 2.3.3. Another one, the PDB file format, is primarily used for storing 3D structure information on biological macromolecules such as proteins and polynucleotides (Tutorial, Section 2.9.7) [52, 53). GIF (Crystallographic Information File) [54, 55] is also a 3D structure information file format with more than three incompatible file versions and is used in crystallography. GIF should not be confused with the Chiron Interchange Formal, which is also extended with. cif. In spectroscopy, JCAMP is apphed as a spectroscopic exchange file format [56]. Here, two modifications can be... [Pg.45]

Solutions of dinitrogen tetroxide (the mixed anhydride of nitric and nitrous acids) in sulphuric acid are nitrating agents ( 4.3.2), and there is no doubt that the effective reagent is the nitronium ion. Its formation has been demonstrated by Raman spectroscopy and by cryoscopy ... [Pg.50]

Tetralin shows evidence in n.m.r. spectroscopy, similar to that mentioned above, for the formation of one or more addition complexes. Tetralin (like indan) is known to undergo acetoxylation. ... [Pg.224]

One of the more obvious changes from the second edition which Modern Spectroscopy has undergone concerns the page size. The consequent new format of the pages is much less crowded and more user friendly. [Pg.470]

Fig. 4. Scanning electron micrograph of 5-p.m diameter Zn powder. Neck formation from localized melting is caused by high-velocity interparticle coUisions. Similar micrographs and elemental composition maps (by Auger electron spectroscopy) of mixed metal coUisions have also been made. Fig. 4. Scanning electron micrograph of 5-p.m diameter Zn powder. Neck formation from localized melting is caused by high-velocity interparticle coUisions. Similar micrographs and elemental composition maps (by Auger electron spectroscopy) of mixed metal coUisions have also been made.
The first quantitative model, which appeared in 1971, also accounted for possible charge-transfer complex formation (45). Deviation from the terminal model for bulk polymerization was shown to be due to antepenultimate effects (46). Mote recent work with numerical computation and C-nmr spectroscopy data on SAN sequence distributions indicates that the penultimate model is the most appropriate for bulk SAN copolymerization (47,48). A kinetic model for azeotropic SAN copolymerization in toluene has been developed that successfully predicts conversion, rate, and average molecular weight for conversions up to 50% (49). [Pg.193]

The formation of such materials may be monitored by several techniques. One of the most useful methods is and C-nmr spectroscopy where stable complexes in solution may give rise to characteristic shifts of signals relative to the uncomplexed species (43). Solution nmr spectroscopy has also been used to detect the presence of soHd inclusion compound (after dissolution) and to determine composition (host guest ratio) of the material. Infrared spectroscopy (126) and combustion analysis are further methods to study inclusion formation. For general screening purposes of soHd inclusion stmctures, the x-ray powder diffraction method is suitable (123). However, if detailed stmctures are requited, the single crystal x-ray diffraction method (127) has to be used. [Pg.74]

However, a second mole of alcohol or hemiformal caimot be added at the ordinary pH of such solutions. The equiUbrium constant for hemiformal formation depends on the nature of the R group of the alcohol. Using nmr spectroscopy, a group of alcohols including phenol has been examined in solution with formaldehyde (15,16). The spectra indicated the degree of hemiformal formation in the order of >methanol > benzyl alcohol >phenol. Hemiformal formation provides the mechanism of stabilization methanol is much more effective than phenol in this regard. [Pg.293]

Reaction with hydrogen is very slight below 800°C, but reduction occurs at higher temperatures. In addition to some SiO formation, the formation of SiOH and SiH groups has been demonstrated by infrared and Raman spectroscopy (96). [Pg.501]

High quahty SAMs of alkyltrichlorosilane derivatives are not simple to produce, mainly because of the need to carefully control the amount of water in solution (126,143,144). Whereas incomplete monolayers are formed in the absence of water (127,128), excess water results in facile polymerization in solution and polysiloxane deposition of the surface (133). Extraction of surface moisture, followed by OTS hydrolysis and subsequent surface adsorption, may be the mechanism of SAM formation (145). A moisture quantity of 0.15 mg/100 mL solvent has been suggested as the optimum condition for the formation of closely packed monolayers. X-ray photoelectron spectroscopy (xps) studies confirm the complete surface reaction of the —SiCl groups, upon the formation of a complete SAM (146). Infrared spectroscopy has been used to provide direct evidence for the hiU hydrolysis of methylchlorosilanes to methylsdanoles at the soHd/gas interface, by surface water on a hydrated siUca (147). [Pg.537]

Tungsten is usually identified by atomic spectroscopy. Using optical emission spectroscopy, tungsten in ores can be detected at concentrations of 0.05—0.1%, whereas x-ray spectroscopy detects 0.5—1.0%. ScheeHte in rock formations can be identified by its luminescence under ultraviolet excitation. In a wet-chemical identification method, the ore is fired with sodium carbonate and then treated with hydrochloric acid addition of 2inc, aluminum, or tin produces a beautiful blue color if tungsten is present. [Pg.284]

The hydrolysis of the uranyl(VI) ion, UO " 2> has been studied extensively and begins at about pH 3. In solutions containing less than lO " M uranium, the first hydrolysis product is the monomeric U02(OH)", as confirmed using time-resolved laser induced fluorescence spectroscopy. At higher uranium concentrations, it is accepted that polymeric U(VI) species are predominant in solution, and the first hydrolysis product is then the dimer, (U02)2(0H) " 2 (154,170). Further hydrolysis products include the trimeric uranyl hydroxide complexes (U02)3(0H) " 4 and (1102)3(OH)(154). At higher pH, hydrous uranyl hydroxide precipitate is the stable species (171). In studying the sol-gel U02-ceramic fuel process, O nmr was used to observe the formation of a trimeric hydrolysis product, ((U02)3( -l3-0)(p.2-0H)3) which then condenses into polymeric layers of a gel based on the... [Pg.326]

Sihcon charge coupled devices (CCDs), commonly used in soHd-state video cameras and in research appHcations, are being appHed to low light level spectroscopy appHcations. The main advantage of area array CCDs over linear photodiode detectors is the two-dimensional format, which provides simultaneous measurements of spatial and spectral data. [Pg.398]

Phenethyl alcohol may be identified as the phenethyl -nitrobenzoate [57455-00-2] (mp 106—108°C), as phenethyl -nitrobenzyl phthalate [65997-34-4] (mp 84.3°C), and also by its formation of styrene on treatment with alkaU. Use of these derivatives has, however, been superseded by physical methods. Infrared (75,76), mass spectroscopy (77), and nmr spectra (78) are useful for identification. [Pg.61]

Combustion chemistry in diffusion flames is not as simple as is assumed in most theoretical models. Evidence obtained by adsorption and emission spectroscopy (37) and by sampling (38) shows that hydrocarbon fuels undergo appreciable pyrolysis in the fuel jet before oxidation occurs. Eurther evidence for the existence of pyrolysis is provided by sampling of diffusion flames (39). In general, the preflame pyrolysis reactions may not be very important in terms of the gross features of the flame, particularly flame height, but they may account for the formation of carbon while the presence of OH radicals may provide a path for NO formation, particularly on the oxidant side of the flame (39). [Pg.519]

Searching. A tmncation feature ( ) that allows word variation, eg, "mass spectrometry or mass spectroscopy" is used. Tide searching is accomphshed by using the added modifier "/ti" to bring up only tides. Commands to retrieve information generally use a protocol such as type-set number/format choice/number of records. [Pg.458]


See other pages where Formation spectroscopy is mentioned: [Pg.353]    [Pg.353]    [Pg.128]    [Pg.481]    [Pg.21]    [Pg.1286]    [Pg.395]    [Pg.472]    [Pg.164]    [Pg.191]    [Pg.240]    [Pg.487]    [Pg.446]    [Pg.18]    [Pg.297]    [Pg.449]    [Pg.428]    [Pg.450]    [Pg.400]    [Pg.410]    [Pg.411]    [Pg.536]    [Pg.203]    [Pg.537]    [Pg.86]    [Pg.327]    [Pg.393]    [Pg.132]    [Pg.165]    [Pg.212]    [Pg.391]   
See also in sourсe #XX -- [ Pg.46 , Pg.218 ]




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Resonance Raman spectroscopy formation

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