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81.
The technique of pulsed laser photolysis was coupled to laser induced fluorescence detection of iodine oxide (IO) to measure rate coefficients, k for the reactions IO + CH(3)O(2)--> products (R1, 30-318 Torr N(2)), IO + CF(3)O(2)--> products (R2, 70-80 Torr N(2)), and IO + O(3)--> OIO + O(2) (R3a). Values of k(1) = (2 +/- 1) x 10(-12) cm(3) molecule(-1) s(-1), k(2) = (3.6 +/- 0.8) x 10(-11) cm(3) molecule(-1) s(-1), and k(3a) <5 x 10(-16) cm(3) molecule(-1) s(-1) were obtained at T = 298 K. In the course of this work, the product yield of IO from the reaction of CH(3)O(2) with I was determined to be close to zero, whereas CH(3)OOI was formed efficiently at 70 Torr N(2). Similarly, no evidence was found for IO formation in the CF(3)O(2) + I reaction. An estimate of the rate coefficients k(CH(3)O(2) + I) = 2 x 10(-11) cm(3) molecule(-1) s(-1) and k(CH(3)OOI + I) = 1.5 x 10(-10) cm(3) molecule(-1) s(-1) was also obtained. The results on k(1)-k(3) are compared to the limited number of previous investigations and the implications for the chemistry of the marine boundary layer are briefly discussed. 相似文献
82.
Direct Oxidative Coupling of N‐Acetyl Indoles and Phenols for the Synthesis of Benzofuroindolines Related to Phalarine 下载免费PDF全文
Terry Tomakinian Dr. Régis Guillot Prof. Dr. Cyrille Kouklovsky Dr. Guillaume Vincent 《Angewandte Chemie (International ed. in English)》2014,53(44):11881-11885
Inspired by the biogenetic synthesis of benzofuroindoline‐containing natural products, we designed an oxidative coupling between phenol and N‐acetyl indoles. This straightforward and direct radical process, mediated by 2,3‐dichloro‐5,6‐dicyano‐1,4‐benzoquinone and FeCl3 allowed the regioselective synthesis of benzofuro[3,2‐b]indolines, whose structure is found in the natural product phalarine. 相似文献
83.
Xu Han Xiwen Chen Terry Gordon Steven Holdcroft 《Macromolecular rapid communications》2009,30(24):2089-2095
A homopolymer of 9,9′‐bis[4‐(2‐(2‐tetrahydropyranyloxy)ethoxy)phenyl]fluorene and its copolymers with 3,4‐benzothiadiazole and 4,7‐di(3(4‐n‐octylphenyl)‐2‐thienyl)‐2,1,3‐benzothiadiazole were synthesized to produce a series of thermally reactive blue, green, and red luminescent polymers. Thermolytic removal of the tetrahydropyran (THP) group from polymer films, rendered the films insoluble due to the formation of hydroxyl groups on the termini of side chains. Thermal removal of the THP was lowered by up to 200 °C, when acid is present in the films. These polymers were found applicable to patterning by NIR direct thermal lithography, in conjunction with a NIR dye and thermal acid generator. The presence of the phenyl groups at the 9‐site carbon was found necessary to eliminate fluorenone formation, and enhance the colour purity of the material.
84.
Filby MH Dickson SJ Zaccheroni N Prodi L Bonacchi S Montalti M Paterson MJ Humphries TD Chiorboli C Steed JW 《Journal of the American Chemical Society》2008,130(12):4105-4113
The synthesis, photophysical, and anion-binding properties of a series of di-, tri-, and tetrapodal anion-binding hosts based on aminopyridinium units with pyrenyl reporter groups are described. The ditopic mesitylene-derived calix[4]arene-based host 4 binds strongly to dicarboxylates, particularly malonate, in a 2:1 anion:host ratio but is essentially nonemissive in the presence of all anions except chloride because of intramolecular quenching by the pyridinium units. Addition of chloride results in a conformational change, giving an initial increase in emission assigned to intramolecular excimer formation. Further chloride addition also results in an increase in the intensity of the pyrenyl monomer emission as chloride binding reduces the acceptor ability of the pyridinium groups. This behavior is not exhibited by control compounds 5 and 6, which lack the ditopic geometry and calixarene spacer unit; however, tripodal 6 forms 1:2 anion:host complexes with a range of anions. 相似文献
85.
86.
87.
Burdzinski GT Gustafson TL Hackett JC Hadad CM Platz MS 《Journal of the American Chemical Society》2005,127(40):13764-13765
Ultrafast laser flash photolysis (266 nm) of para- and ortho-biphenyl azide in acetonitrile produces azide excited states that have broad absorption bands centered at 480 nm. The para-biphenyl azide excited singlet state has a lifetime of 100 fs. The excited-state lifetime of the ortho-azide isomer is 450 +/- 150 fs. Decay of the azide excited states is accompanied by the formation of the corresponding known singlet nitrenes (para, lambdamax = 350 nm, ortho, lambdamax = 400 nm). Singlet para-biphenylnitrene is born with excess energy and undergoes vibrational cooling with a time constant of 11 ps to form the long-lived (tau approximately 9 ns) relaxed singlet nitrene. Singlet ortho-biphenylnitrene decays with a lifetime of 16 ps in acetonitrile at ambient temperature. 相似文献
88.
Lowe Terry C. Bishop Alan Burns Carol Hartford Allen Parkin Don Trewhella Jill 《Journal of nanoparticle research》2000,2(3):249-266
Research in the emerging field of nanoscale science and technology has grown steadily at Los Alamos National Laboratory since 1990. This article summarizes some of this work, examining research highlights within the seven key categories of nanoscience in which Los Alamos has ongoing projects, capabilities, and facilities: (1) Materials and chemistry, (2) Theory and modeling, (3) Bioscience, (4) Investigative tools and facilities, (5) Sensors and devices, (6) Synthesis and fabrication, and (7) Education and outreach. Future research horizons are indicated throughout while institutional strategies for advancing nanoscale science are summarized at the end. 相似文献
89.
Terry Bradfield 《General Relativity and Gravitation》1989,21(7):665-675
In this paper we present a new method for constructing theories of gravitation which exhibit spontaneously broken conformal symmetry. It does not require introducing nongeometric terms (i.e., auxiliary gauge fields or potential terms for the conformal field) into the Lagrangian. It is based on a theory which initially is locally both Lorentz invariant and Weyl gauge invariant inD dimensions. It is shown that, if the field Lagrangian contains terms quadratic in curvature in addition to the Ricci scalar, then the field equations allow both the dilation field and some connection components to have nonvanishing vacuum values. Both Lorentz and Weyl symmetries are thereby broken simultaneously. 相似文献
90.
K.A. Schmidt M. Bergström G.B. Hagemann B. Herskind G. Sletten P.G. Varmette J. Domscheit H. Hübel S.W. Ødegård S. Frattini A. Bracco B. Million M.P. Carpenter R.V.F. Janssens T.L. Khoo T. Lauritsen C.J. Lister S. Siem I. Wiedenhöver D.J. Hartley L.L. Riedinger A. Maj W.C. Ma R. Terry 《The European Physical Journal A - Hadrons and Nuclei》2001,12(1):15-28
High-spin properties of the nucleus 169Hf have been studied through the fusion evaporation reaction 96Zr(76Ge,3n)169Hf at a beam energy of 310 MeV. The known rotational bands have been extended considerably and 6 new bands have been established,
four of which form coupled bands with pronounced M1 connections. Quasiparticle assignments are suggested for the new band structures, and it appears that coupling to vibrational
degrees of freedom plays a role. Both coupled bands involve the excitation of quasiprotons. In the region of highest spin,
a large alignment gain is interpreted in terms of a mixed crossing where an h
9/2 and an h
11/2 quasiproton provide the two signatures of the aligning configuration.
Received: 23 March 2001 / Accepted: 20 September 2001 相似文献