21,812 research outputs found
A possible mechanism of superconductivity in high-T-c cuprates
No full textThis paper derives a generic T-c formula by using the long-range phase coherence condition in quantum phase fluctuation of the order parameter. Taking the two-local-spin-mediated interaction (TLSMI) proposed by Liu and Chen [Phys. Rev. B 58 (1998) 8812] as a Cooper pair potential, and the T-c formula, this paper explains five basic experimental facts in high-T-c cuprates. The aim of this paper is to show that TLSMI is a possible pairing mechanism of superconductivity in high-T-c cuprates. (C) 2000 Elsevier Science B.V. All rights reserved.Physics, AppliedSCI(E)EI0ARTICLE4276-28434
Test Make Sense?
No full textCorresponding author Changyu Liu should be listed as the first corresponding author.No Full Tex
Electrochemical behavior of diazirines
No full textPT: J; CR: ENGEL PS, 1980, CHEM REV, V80, P99 FRY AJ, 1973, J ORG CHEM, V38, P2620 KITAJEV JP, 1965, COLLECT CZECH CHEM C, V30, P4178 LIU MTH, 1981, J CHEM SOC P2, P53 LUND H, 1966, COLLECT CZECH CHEM C, V31, P4175 MALACHESKY PA, 1969, ANAL CHEM, V41, P1493 MOFFAT JB, 1978, CHEM DIAZONIUM DIA 1 NICHOLSON RS, 1964, ANAL CHEM, V36, P706 SCHWARZ WM, 1965, J PHYS CHEM-US, V69, P30; NR: 9; TC: 2; J9: J CHEM SOC CHEM COMMUN; PG: 2; GA: NJ399Source type: Electronic(1
Insertion of phenylchlorocarbenes in the C-H bonds of alkanes: measurement of the rate constants by laser flash photolysis
No full textPhenylchlorocarbenes, produced by photolysis of the parent diazirines, have a very limited lifetime in alkane solvents. The rate of disappearance of p-methyl- and p-chlorophenylchlorocarbenes has been measured in iso-octane, cyclohexane and n-hexane as well as in benzene for comparison. The rate constants of several processes (dimerization, addition to the diazirine, reaction with the solvent, etc. ) contributing to the disappearance of the phenylchlorocarbenes have been determined. The rate of reaction with the solvent, which is much lower in benzene than in alkanes and depends strongly on the nature of the alkane, is assumed to be an insertion of the carbene in the C-H bonds of the solvent. Consequences of this reaction on the chemistry of carbenes produced by continuous irradiation (or thermolysis) of diazirines in alkanes are briefly discussed.PT: J; CR: BENSASSON R, 1971, T FARADAY SOC, V67, P1904 BONNEAU R, 1986, NOUV J CHIM, V10, P425 BONNEAU R, 1991, PURE APPL CHEM, V63, P289 DOYLE MP, 1988, TETRAHEDRON LETT, V29, P5863 GOULD IR, 1985, TETRAHEDRON, V41, P1587 GRAHAM WH, 1965, J AM CHEM SOC, V87, P4396 LIU MTH, 1987, CHEM DIAZIRINES LIU MTH, 1990, J CHEM SOC CHEM COMM, P1482 LIU MTH, 1992, J AM CHEM SOC, V114, P3604 LIU MTH, 1992, J ORG CHEM, V57, P2483 LIU MTH, 1992, J PHOTOCH PHOTOBIO A, V63, P115 LUTZ H, 1973, J PHYS CHEM-US, V77, P1758 MORGAN S, 1991, J AM CHEM SOC, V113, P2782 MOSS RA, 1990, J AM CHEM SOC, V112, P5642 MOSS RA, 1990, KINETICS SPECTROSCOP; NR: 15; TC: 11; J9: J PHOTOCHEM PHOTOBIOL A-CHEM; PG: 10; GA: JQ196Source type: Electronic(1
liu-temporal-processing-dataset
No full textBehavioral analysis processed dataset accompanying the paper "Temporal processing and context dependency in *C. elegans* mechanosensation"See README.md for more details.</div
Jia ru ju he wu dui jun yun tuan liu ji jun yun tuan liu dui liu de ying xiang
No full textWong, Chai Kwok = 加入聚合物對均勻湍流及均勻湍流對流的影響 / 黃濟國.Thesis M.Phil. Chinese University of Hong Kong 2013.Includes bibliographical references (leaves 89-91).Abstracts also in Chinese.Title from PDF title page (viewed on 01, November, 2016).Wong, Chai Kwok = Jia ru ju he wu dui jun yun tuan liu ji jun yun tuan liu dui liu de ying xiang / Huang Jiguo
Benzylchlorocarbene: origins of Arrhenius curvature in the kinetics of the 1,2-H shift rearrangement
No full textBenzylchlorocarbene (1, BCC) was generated photochemically from benzylchlorodiazirine (2) in isooctane, methylcyclohexane (MCH), and tetrachloroethane (TCE) at temperatures from similar to 30 to -75 degrees C. At -70 degrees C in isooctane, the identified products included Z/E-beta-chlorostyrenes 4 (46.6%), alpha-chlorostyrene 5 (2.4%), 1,1-dichloro-2-phenylethane 6 (1.9%), a BCC-isooctane insertion product 8 (5.5%), carbene dimers 9 (3.8%), and azine 3 (30%). The significant incursion of intermolecular products 3, 8, and 9 implies that laser flash photolytic (LFP) kinetic data for the decay of BCC obtained at low temperature is biased and should not be employed in Arrhenius analyses. Accordingly, previously obtained curved Arrhenius correlations for BCC do not necessarily implicate quantum mechanical tunneling (QMT) in the 1,2-H shift rearrangement of BCC to 4. Similarly in MCH, where BCC affords a solvent insertion product in similar to 44-53% yield, the curved Arrhenius correlation (Figure 1) cannot be readily interpreted. In polar solvents such as TCE, clean H-shift reactions of BCC are obtained even at -71 degrees C; an Arrhenius correlation of LFP kinetic data is linear from 3 to -71 degrees C (Figure 2), affording E-a = 3.2 kcal mol(-1) and log A = 10.0 s(-1). Therefore, QMT does not appear to play a major role in the 1,2-H shift rearrangement of BCC at ambient or near ambient temperature in solution.PT: J; CR: BONNEAU R, 1996, J AM CHEM SOC, V118, P3829 DEAN JA, 1992, LANGES HDB CHEM DIX EJ, 1993, J AM CHEM SOC, V115, P10424 DOX AW, 1941, ORG SYNTH, V1, P5 GRAHAM WH, 1965, J AM CHEM SOC, V87, P4396 ISAACS NS, 1995, PHYSICAL ORGANIC CHE, P304 JACKSON JE, 1988, J AM CHEM SOC, V110, P5595 KAZANIS S, 1991, J PHYS CHEM-US, V95, P4430 KEATING AE, 1997, COMMUNICATION 0804 LAVILLA JA, 1989, J AM CHEM SOC, V111, P6877 LAVILLA JA, 1990, TETRAHEDRON LETT, V31, P5109 LIU MTH, 1984, TETRAHEDRON, V40, P887 LIU MTH, 1985, CHEM COMMUN, P982 LIU MTH, 1985, J ORG CHEM, V50, P3218 LIU MTH, 1990, J AM CHEM SOC, V112, P3915 LIU MTH, 1992, J AM CHEM SOC, V114, P3604 LIU MTH, 1992, J PHOTOCH PHOTOBIO A, V63, P115 LIU MTH, 1994, ACCOUNTS CHEM RES, V27, P287 LIU MTH, 1994, J PHOTOCH PHOTOBIO A, V84, P133 MODARELLI DA, 1992, J AM CHEM SOC, V114, P7034 MODARELLI DA, 1993, J AM CHEM SOC, V115, P470 MOSS RA, 1987, J AM CHEM SOC, V109, P4341 MOSS RA, 1990, J AM CHEM SOC, V112, P1638 MOSS RA, 1994, ADV CARBENE CHEM, V1, P59 MOSS RA, 1996, J AM CHEM SOC, V118, P12588 MOSS RA, 1997, CHEM COMMUN 0321, P617 MOSS RA, 1997, TETRAHEDRON LETT, V38, P7049 STORER JW, 1993, J AM CHEM SOC, V115, P10426 SUGIYAMA MH, 1992, J AM CHEM SOC, V114, P966 TOMIOKA H, 1984, J AM CHEM SOC, V106, P454 WHITE WR, 1992, J ORG CHEM, V57, P2841 WIERLACHER S, 1993, J AM CHEM SOC, V115, P8943 YEN VQ, 1962, ANN CHIM, V7, P785; NR: 33; TC: 8; J9: J ORG CHEM; PG: 7; GA: ZM109Source type: Electronic(1
Reaction of 3-chloro-3-methyldiazirines with hydrogen atoms
No full textPT: J; CR: BINGHAM RC, 1975, J AM CHEM SOC, V97, P1285 BRADLEY GF, 1977, J CHEM SOC P2, P1214 BRASLAVSKY S, 1977, CHEM REV, V77, P473 CHADWELL HM, 1933, J AM CHEM SOC, V55, P1363 CLARK DT, 1969, T FARADAY SOC, V62, P393 CLARK DT, 1969, T FARADAY SOC, V62, P399 CLARK DT, 1969, T FARADAY SOC, V62, P405 CLOUGH PN, 1970, CAN J CHEM, V48, P2919 DYKSTRA CE, 1978, J AM CHEM SOC, V100, P1378 FIGUERA JM, 1978, J CHEM SOC F1, P809 FREY HM, 1966, ADV PHOTOCHEM, V4, P225 FREY HM, 1977, J CHEM SOC F1, P2010 GILBERT JC, 1979, TETRAHEDRON LETT, P4619 GRAHAM WH, 1965, J AM CHEM SOC, V87, P4306 JAMIESON JWS, 1970, CAN J CHEM, V48, P3619 JENNINGS BM, 1976, J AM CHEM SOC, V98, P6416 JONES M, 1973, CARBENES, V1 JONES WE, CHEM BIOMED ENV INST JONES WE, 1973, CHEM REV, V73, P407 JONES WE, 1978, J CHEM SOC F2, V74, P831 LAU A, 1964, SPECTROCHIM ACTA, V20, P97 LIU MTH, UNPUBLISHED LIU MTH, 1973, CAN J CHEM, V51, P2393 LIU MTH, 1977, CAN J CHEM, V55, P3596 MAEDA Y, 1979, J AM CHEM SOC, V101, P837 MARTIN LR, 1979, INT J CHEM KINET, V11, P543 MEIER H, 1977, ANGEW CHEM INT EDIT, V16, P835 MOFFAT JB, 1978, CHEM DIAZONIUM DIA 1 MOSS RA, 1978, J CHEM SOC CHEM COMM, P775 SCHMITZ E, 1964, ANGEW CHEM INT EDIT, V3, P333 SCHMITZ E, 1971, 23RD INT C PUR ALL C, V2, P283 SCOTT PM, 1969, J PHYS CHEM-US, V73, P1513 SMITH NP, 1979, J CHEM SOC P2, P213 WITTER RA, 1973, J ORG CHEM, V38, P484; NR: 34; TC: 3; J9: J AMER CHEM SOC; PG: 2; GA: JN379Source type: Electronic(1
Afrotropical Centistidea Rohwer, 1914 (Hymenoptera, Braconidae) with description of four new species
No full textThe braconid parasitoid wasp genus Centistidea Rohwer, 1914 is revised for the Afrotropical region, with four new species described; Centistidea areolaris Liu &amp; Polaszek, sp. nov., C. linearis Liu &amp; Polaszek, sp. nov., C. longipedes Liu &amp; Polaszek, sp. nov., and C. turneri Liu &amp; Polaszek, sp. nov. are described based on specimens from the Natural History Museum, United Kingdom, and the Royal Museum for Central Africa, Belgium. An illustrated key to species in the Afrotropical region is provided
Determination of the photolytic decomposition pathways of benzylchlorodiazirine by C60 probe technique
No full textBy employing C-60 as a chemical probe, the photolysis of benzylchlorodiazirine has been proposed to form carbene and the rearranged products via the excited state. (c) 2006 Elsevier Ltd. All rights reserved.PT: J; CR: AKASAKA T, 1999, ORG LETT, V1, P1509 AKASAKA T, 2000, J AM CHEM SOC, V122, P7134 FREY HM, 1965, J CHEM SOC, P1700 GRAHAM WH, 1965, J AM CHEM SOC, V87, P4396 HIRSCH A, 1993, CHEM BER, V126, P1061 ISHITSUKA MO, 2004, TETRAHEDRON LETT, V45, P6321 KORSHUNOVA GA, 2000, MOL BIOL+, V34, P823 LIU MTH, 1985, J CHEM SOC CHEM COMM, P982 LIU MTH, 1987, CHEM DIAZIRINES, V1 LIU MTH, 1987, CHEM DIAZIRINES, V2 LIU MTH, 1990, J AM CHEM SOC, V112, P3915 LIU MTH, 1992, J AM CHEM SOC, V114, P3604 LIU MTH, 2003, J ORG CHEM, V68, P7471 MODARELLI DA, 1992, J AM CHEM SOC, V114, P7034 NIGAM M, 1998, J AM CHEM SOC, V120, P8055 RICHARDS FM, 2000, PROTEIN SCI, V9, P2506 TOMIOKA H, 1984, J AM CHEM SOC, V106, P454 WAKAHARA T, 2002, J AM CHEM SOC, V124, P9465; NR: 18; TC: 0; J9: TETRAHEDRON LETT; PG: 3; GA: 130SPSource type: Electronic(1
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