Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Species identifying

Efforts by various investigators to demonstrate a luciferin-luciferase reaction with luminous fungi were uniformly unsuccessful until Airth and McElroy (1959) obtained a positive result. Airth s group studied further details of the luciferin-luciferase reaction using the luciferin preparation obtained from Armillaria mellea and the luciferase preparation obtained from a species identified by them... [Pg.268]

PIE curves for ra/z = 72 (C4H8O) measured in four butanol flames. The accepted ionization energies for species identified by the observed ionization thresholds are indicated. (From Yang, B. et at. Combust. Flame, 148,198, 2007. With permission.)... [Pg.11]

The Lewis structures verity that each species identified as a Lewis base possesses lone pairs of electrons and that the Lewis acids have orbitals available to accept electrons. [Pg.1505]

Assuming limited resomces, the wildlife component of a mercmy monitoring network would likely have to rely on analyses of tissue from a small subset of candidate species identified earlier in this chapter, so identification of key species that both meet the criteria as good current indicators (see Section 5.5) as well as... [Pg.160]

Fig. 3.13 151 GHz Spectrum (excerpt) from the nucleus of the molecular cloud G 327.3-0.6 in the southern sky. The molecular species identified are shown. Peaks which are not labelled are not yet clearly identified. (The numbers used to label the molecular cloud, G 327.3-0.6, are galactic coordinates). With personal permission of Prof. Hjalmarsson, Chalmers University of Technology, Goteborg, Sweden, from the Proceedings of the First European Workshop on Exo/Astrobiology, Frascati, 21-23 May 2001, ESA SP-496... Fig. 3.13 151 GHz Spectrum (excerpt) from the nucleus of the molecular cloud G 327.3-0.6 in the southern sky. The molecular species identified are shown. Peaks which are not labelled are not yet clearly identified. (The numbers used to label the molecular cloud, G 327.3-0.6, are galactic coordinates). With personal permission of Prof. Hjalmarsson, Chalmers University of Technology, Goteborg, Sweden, from the Proceedings of the First European Workshop on Exo/Astrobiology, Frascati, 21-23 May 2001, ESA SP-496...
Holland and Peters earlier reported examples of three- and four-coordinate N2 complexes with iron in the formal +1 oxidation state, but in neither case were terminally bonded N2 species identified or isolated dinuclear end-on Fe-NN-Fe species were inevitably obtained (99,100). Therefore, Peters and coworkers recently began to turn their attention to new derivatives of the classic Sacconi-type tripodal ligands to achieve access to a terminally bound Fe-N2 complex. Indeed, by employing the mono-anionic ligand L8 — [f2-Ph2PC6H4)3Si] (Fig. 10) they were able to generate the desired complex [Fe(L8)(N2)] (10) (101). [Pg.415]

In 1987 we reported26 that the three possible C3H2 isomers S-2, T-36, and S-37 can be transformed into each other under photochemical conditions. For several reasons propargylene (36) attracted our attention On the one hand the first C3H2 parent species, identified by direct spectroscopic methods, was triplet propargylene (T-36). Its ESR spectrum was published in 1965,63 and, based on the zero-field-splitting parameters, a linear or nearly linear structure was derived. On the other hand, the structural elucidation of 36 by comparison of the calculated and experimental IR spectra turned out to be rather difficult.64... [Pg.126]

The species identified as XA reacts with styrene to give the expected cyclopropane. The rate constant for this reaction is ca 200 times less than the corresponding rate constant for 3BA (Table 6). Also, use of the deuterium-labeled a-methylstyrene reveals that the cyclopropanation occurs with essentially total retention of stereochemistry. Moreover, precisely the same result is obtained when this carbene is formed by triplet sensitization rather than by direct irradiation. These findings also point to a reaction originating from a singlet carbene. [Pg.339]

Microbe Mesophitic initial temp. < 40°C Thermophilic 40-70°C Mesophilic 70°C to cooler Number of species identified... [Pg.329]

Species identified by matrix isolation include cyclobutadiene and benzyne, where products derived from these molecules are formed at higher temperatures. [Pg.195]

The sex pheromones of four Plusiinae species in the family Noctu-idae namely, Ctenoplusia albostriata (CA), Macdunnoughiapurissima (MP), Syngrapha ain (SA) and Diachrysia stenochrysis (DS), were identified. CA females produced ( )-5-decenyl acetate (1), ( )-7-dodecenyl acetate (II), and (.Z)-7-dodecen-l-ol (III) in a ratio of 2 100 13. The MP females produce II, III, and ( )-5-dodecenyl acetate (IV) in a ratio of 100 80 20. Compounds 11 and 111 were also identified from the SA females, whereas the DS females produced just one active compound, (.Z)-7-decenyl acetate. DS species were the first Plusiinae species identified using only the oo3-compound and none of the oo5-compounds, such as II and III that are common components of Plusiinae pheromones. [Pg.302]

In the earlier volume of this book, the chapter dedicated to transition metal peroxides, written by Mimoun , gave a detailed description of the features of the identified peroxo species and a survey of their reactivity toward hydrocarbons. Here we begin from the point where Mimoun ended, thus we shall analyze the achievements made in the field in the last 20 years. In the first part of our chapter we shall review the newest species identified and characterized as an example we shall discuss in detail an important breakthrough, made more than ten years ago by Herrmann and coworkers who identified mono- and di-peroxo derivatives of methyl-trioxorhenium. With this catalyst, as we shall see in detail later on in the chapter, several remarkable oxidative processes have been developed. Attention will be paid to peroxy and hydroperoxide derivatives, very nnconunon species in 1982. Interesting aspects of the speciation of peroxo and peroxy complexes in solntion, made with the aid of spectroscopic and spectrometric techniqnes, will be also considered. The mechanistic aspects of the metal catalyzed oxidations with peroxides will be only shortly reviewed, with particular attention to some achievements obtained mainly with theoretical calculations. Indeed, for quite a long time there was an active debate in the literature regarding the possible mechanisms operating in particular with nucleophilic substrates. This central theme has been already very well described and discussed, so interested readers are referred to published reviews and book chapters . [Pg.1057]

Figure 1.5 is an E-pH diagram for Al under standard conditions. This means that all soluble species are at LOOM, the species being Al+ and Al(OH)4. The labels for the four species identify the regions in which they predominate under differing E and pH conditions. These predominance conditions may be seen by examination of the three vertical lines in Figure 1.6 and the three horizontal lines in Figure 1.7. Start at the top of the vertical line at a constant pH of 0.0. As one goes down the line, the predominant species Al+ gives way to the predominant species Al at an E value of about —1.7 v. The reduction halfreaction is written as follows with the E° value as obtained from appropriate tables attached. Figure 1.5 is an E-pH diagram for Al under standard conditions. This means that all soluble species are at LOOM, the species being Al+ and Al(OH)4. The labels for the four species identify the regions in which they predominate under differing E and pH conditions. These predominance conditions may be seen by examination of the three vertical lines in Figure 1.6 and the three horizontal lines in Figure 1.7. Start at the top of the vertical line at a constant pH of 0.0. As one goes down the line, the predominant species Al+ gives way to the predominant species Al at an E value of about —1.7 v. The reduction halfreaction is written as follows with the E° value as obtained from appropriate tables attached.
Infrared and Raman spectroscopy. Stephens and Price (1970, 1972) used infrared spectroscopy to examine both ambient and laboratory-generated aerosols. They identified sulfate, nitrate, and ammonium ion absorption bands in ambient particles as well as bands indicating the presence of organics in diesel exhaust (C-H) and oxidized organics in irradiated hydrocarbon-NO, . mixtures. Since then, many studies using IR have been carried out and a variety of species identified, including COf , PO4-, and SiO A See Chapter 9.C.2 and Figs. 9.49, 9.50, and 9.51 for some typical FTIR spectra of atmospheric particles. [Pg.623]

Fig. 1.4 Diagram showing the principle of operation of a time-of-flight atom-probe. The tip is mounted on either an internal or an external gimbal system. The tip orientation is adjusted so that atoms of one s choice for chemical analysis will have their images falling into the small probe-hole at the screen assembly. By pulse field evaporating surface atoms, these atoms, in the form of ions, will pass through the probe hole into the flight tube, and be detected by the ion detector. From their times of flight, their mass-to-charge ratios are calculated, and thus their chemical species identified. Fig. 1.4 Diagram showing the principle of operation of a time-of-flight atom-probe. The tip is mounted on either an internal or an external gimbal system. The tip orientation is adjusted so that atoms of one s choice for chemical analysis will have their images falling into the small probe-hole at the screen assembly. By pulse field evaporating surface atoms, these atoms, in the form of ions, will pass through the probe hole into the flight tube, and be detected by the ion detector. From their times of flight, their mass-to-charge ratios are calculated, and thus their chemical species identified.

See other pages where Species identifying is mentioned: [Pg.115]    [Pg.418]    [Pg.375]    [Pg.388]    [Pg.615]    [Pg.141]    [Pg.443]    [Pg.236]    [Pg.142]    [Pg.33]    [Pg.253]    [Pg.74]    [Pg.255]    [Pg.132]    [Pg.130]    [Pg.131]    [Pg.289]    [Pg.56]    [Pg.177]    [Pg.3]    [Pg.126]    [Pg.243]    [Pg.305]    [Pg.359]    [Pg.397]    [Pg.162]    [Pg.47]    [Pg.9]    [Pg.33]    [Pg.303]    [Pg.1057]    [Pg.461]    [Pg.290]    [Pg.292]    [Pg.205]    [Pg.324]   
See also in sourсe #XX -- [ Pg.269 ]




SEARCH



© 2024 chempedia.info