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41.
Exposure of isolated photosystem I (PSI) complexes to illumination (2300 microE m(-2) s(-1)) for various periods of time resulted in striking changes in their absorption spectra. A 6 nm blueshift of the absorption maximum in the red was detected after 100 min illumination. The fourth derivative of the absorption spectra verifies that the main change of the red peak was attributed to the 682 nm absorption band. Further, it was also shown that a shoulder in the absorption spectra located around 470 nm decreased after the first 5 min of illumination and almost disappeared after 40 min illumination, suggesting that chlorophyll b bound to light-harvesting complex I (LHCI) is also sensitive to excess light. A maximum inhibitory effect on the oxygen uptake rates and a strong stimulation were observed when the PSI complexes were exposed to illumination for about 20 and 40 min, respectively. Sodium dodecyl sulfate-polyacrylamide gel electrophoresis shows that LHCI-680 started to degrade during the first 5 min of illumination and almost completely disappeared after 40 min of illumination. These observations demonstrated that LHCI was more sensitive to illumination than the PsaA/B subunits which also presented some degradation signs after 40 min illumination. In addition, insoluble-cohesive-denatured proteins also appeared between the stacking and resolving gel after prolonged illumination (100 min). A photoprotective function of LHCI for the PSI reaction center is proposed. 相似文献
42.
Hanin S Adam P Kowalewski I Huc AY Carpentier B Albrecht P 《Chemical communications (Cambridge, England)》2002,(16):1750-1751
Two bridgehead-alkylated 2-thiaadamantanes (1,5-dimethyl and 1-methyl) have been identified in petroleum; these compounds give clues to sulfurisation processes affecting petroleum which has undergone high thermal stress. 相似文献
43.
Carpentier L. Bourgeois L. Descamps M. 《Journal of Thermal Analysis and Calorimetry》2002,68(2):727-739
The temperature modulated differential scanning calorimetry (MDSC®) technique has been used to characterise the low frequency molecular mobility of indomethacin and maltitol just above their respective calorimetric glass transition temperatureT g. Analysis has been made using the concept of complex specific heat. Spectroscopic information are thus obtained through the temperature dependence of the isochronal real and imaginary parts C′ and C″. This gives access to the fragility index m and the stretched exponent β. The comparison with dielectric spectroscopy has been performed to check the coherence of spectroscopic information. Measurements on maltitol enable to demonstrate the useful complementarity of the technique when the low frequencies dielectric relaxations are occulted by the presence of conductors default. 相似文献
44.
Clémence Guillaume Noureddine Ajellal Jean‐François Carpentier Sophie M. Guillaume 《Journal of polymer science. Part A, Polymer chemistry》2011,49(4):907-917
The controlled ring‐opening polymerization of racemic allyl‐β‐butyrolactone (rac‐BLallyl) in toluene or in bulk, catalyzed by the discrete β‐diiminate zinc amido [(BDIiPr)Zn(N(SiMe3)2)] ( 1 ) or {amino‐methoxy‐bis(phenolate)}yttrium amido [(ONOOtBu)Y(N(SiHMe2)2)(THF)] ( 2 ) complexes, in association with an alcohol, gave poly(β‐hydroxyalkanoate)s (PHAs) with allylic side chains. These PHAsallyl exhibit either a slightly isotactic‐enriched (Pm = 0.61) or highly syndiotactic‐enriched (Pr = 0.82) backbone structure, respectively, with high molar mass (M n up to 21,100 g mol?1) and narrow molar mass distribution values (1.05 < M w/M n < 1.28), as evidenced by detailed 13C NMR and size exclusion chromatography analyses. Postpolymerization rhodium‐catalyzed hydroboration of the resulting PHAsallyl with pinacolborane quantitatively afforded the corresponding PHAsboron. Introduction of boron into the pendant chains did not alter neither the structure of the polymer backbone nor the macromolecular features (M n, M w/M n, and stereoregularity). However, differential scanning calorimetry analyses revealed a significant increase of the glass transition temperature on modifying the allyl for the boron function in these PHAs. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2011 相似文献
45.
Sequential Barium‐Catalysed N−H/H−Si Dehydrogenative Cross‐Couplings: Cyclodisilazanes versus Linear Oligosilazanes
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Clément Bellini Dr. Thierry Roisnel Prof. Dr. Jean‐François Carpentier Dr. Sven Tobisch Dr. Yann Sarazin 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(44):15733-15743
Starting from Ph3SiH, the barium precatalyst Ba[CH(SiMe3)2]2?(THF)3 was used to produce the disilazane Ph3SiN(Bn)SiPh2NHBn ( 4 ) by sequential N?H/H?Si dehydrogenative couplings with BnNH2 and Ph2SiH2. Substrate scope was extended to other amines and hydrosilanes. This smooth protocol gives quantitative yields and full chemoselectivity. Compound 4 and the intermediates Ph3SiNHBn and Ph3SiN(Bn)SiHPh2 were structurally characterised. Further attempts at chain extension by dehydrocoupling of Ph2SiH2 with 4 instead resulted in cyclisation of this compound, forming the cyclodisilazane c‐(Ph2Si‐NBn)2 ( 5 ) which was crystallographically authenticated. The ring‐closure mechanism leading to 5 upon release of C6H6 was determined by complementary experimental and theoretical (DFT) investigations. Ba[CH(SiMe3)2]2?(THF)3 and 4 react to afford the reactive Ba{N(Bn)SiPh2N(Bn)SiPh3}2, which was characterised in situ by NMR spectroscopy. Next, in a stepwise process, intramolecular nucleophilic attack of the metal‐bound amide on the terminal silicon atom generates a five‐coordinate silicate. It is followed by turnover‐limiting β‐C6H5 transfer to barium; this releases 5 and forms a transient [Ba]?Ph species, which undergoes aminolysis to regenerate [Ba]?N(Bn)SiPh2N(Bn)SiPh3. DFT computations reveal that the irreversible production of 5 through such a stepwise ring‐closure mechanism is much more kinetically facile (ΔG≠=26.2 kcal mol?1) than an alternative σ‐metathesis pathway (ΔG≠=48.2 kcal mol?1). 相似文献
46.
Dr. Bo Liu Dr. Thierry Roisnel Prof. Dr. Jean‐François Carpentier Dr. Yann Sarazin 《Chemistry (Weinheim an der Bergstrasse, Germany)》2013,19(8):2784-2802
The behavior of the first aminophenolate catalysts of the large alkaline earth metals (Ae) [(LOi)AeN(SiMe2R)2(thf)x] (i=1–4; Ae=Ca, Sr, Ba; R=H, Me; x=0–2) for the cyclohydroamination of terminal aminoalkenes is discussed. The complexes [(BDI)AeN(SiMe2H)2(thf)x] (Ae=Ca, Sr, Ba, x=1–2; (BDI)H=H2C[C(Me)N‐2,6‐(iPr)2C6H3]2)) and [(BDI)CaN(SiMe3)2(thf)] supported by the β‐diketiminate (BDI)? ligand have also been employed for comparative and mechanistic considerations. The catalytic performances decrease in the order Ca>Sr?Ba, which is the opposite trend to that previously observed during the intermolecular hydroamination of activated alkenes catalyzed by the same alkaline‐earth metal complexes. Catalyst efficacy increases when the chelating and donating ability of the aminophenolate ligands decreases. For given metals and ancillary scaffolds, disilazide catalysts that incorporate the N(SiMe3)2? amido group outclass their congeners containing the N(SiMe2H)2? amide owing to the lower basicity of the N(SiMe2H)2? with respect to the N(SiMe3)2? group, and also because Ae–N(SiMe2H)2 catalysts suffer from irreversible deactivation through the dehydrogenative coupling of amine and hydrosilane moieties. This deactivation process takes place at 25 °C in the case of [(LOi)AeN(SiMe2H)2(thf)x] phenolate complexes and occurs even with the related [(BDI)AeN(SiMe2H)2(thf)x] complex, albeit under conditions harsher than those required for effective cyclohydroamination catalysis. A mechanistic scenario for cyclohydroamination catalyzed by [(LX)AeN(SiMe2H)2(thf)x] complexes ((LX)?=(LOi)? or (BDI)?) is proposed. Although beneficial for the synthesis of Ae heteroleptic complexes able to resist deleterious Schlenk‐type equilibria, the use of the N(SiMe2H)2? is prejudicial to catalytic activity in the case of catalyzed transformations that involve reactive amine (and potentially other) substrates. Mechanistic and kinetic investigations further illustrate the interplay between the catalytic activity, operative mechanism, and identity of the metal, ancillary ligand, and amido group. These studies suggest that the widely accepted mechanism for cyclohydroamination reactions cannot be extended systematically to all alkaline‐earth catalysts. The [(BDI)CaN(SiMe2H)2{H2NCH2C(CH3)2CH2CH?CH2}2] complex, the first Ca–aminoalkene adduct structurally characterized, was prepared quantitatively and essentially behaves like [(BDI)CaN(SiMe2H)(thf)], thus serving as a model compound for mechanistic studies, as illustrated during stoichiometric reactions monitored by 1H NMR spectroscopy. 相似文献
47.
Dr. Bo Liu Dr. Thierry Roisnel Prof. Dr. Jean‐François Carpentier Dr. Yann Sarazin 《Chemistry (Weinheim an der Bergstrasse, Germany)》2013,19(40):13445-13462
[{N^N}M(X)(thf)n] alkyl (X=CH(SiMe3)2) and amide (X=N(SiMe3)2) complexes of alkaline earths (M=Ca, Sr, Ba) and divalent rare earths (YbII and EuII) bearing an iminoanilide ligand ({N^N}?) are presented. Remarkably, these complexes proved to be kinetically stable in solution. X‐ray diffraction studies allowed us to establish size–structure trends. Except for one case of oxidation with [{N^N}YbII{N(SiMe3)2}(thf)], all these complexes are stable under the catalytic conditions and constitute effective precatalysts for the cyclohydroamination of terminal aminoalkenes and the intermolecular hydroamination and intermolecular hydrophosphination of activated alkenes. Metals with equal sizes across alkaline earth and rare earth families display almost identical apparent catalytic activity and selectivity. Hydrocarbyl complexes are much better catalyst precursors than their amido analogues. In the case of cyclohydroamination, the apparent activity decreases with metal size: Ca>Sr>Ba, and the kinetic rate law agrees with RCHA=k[precatalyst]1[aminoalkene]1. The intermolecular hydroamination and hydrophosphination of styrene are anti‐Markovnikov regiospecific. In both cases, the apparent activity increases with the ionic radius (Ca<Sr<Ba) but the rate laws are different, and obey RHA=k[styrene]1[amine]1[precatalyst]1 and RHP=k[styrene]1[HPPh2]0[precatalyst]1, respectively. Mechanisms compatible with the rate laws and kinetic isotopic effects are proposed. [{N^N}Ba{N(SiMe3)2}(thf)2] ( 3 ) and [{N^N}Ba{CH(SiMe3)2}(thf)2] ( 10 ) are the first efficient Ba‐based precatalysts for intermolecular hydroamination and hydrophosphination, and display activity values that are above those reported so far. The potential of the precatalysts for C? N and C? P bond formation is detailed and a rare cyclohydroamination–intermolecular hydroamination “domino” sequence is presented. 相似文献
48.
Dr. Lingfang Wang Dr. Christos E. Kefalidis Dr. Sourisak Sinbandhit Dr. Vincent Dorcet Prof. Dr. Jean‐François Carpentier Prof. Dr. Laurent Maron Dr. Yann Sarazin 《Chemistry (Weinheim an der Bergstrasse, Germany)》2013,19(40):13463-13478
The tin(II) complexes {LOx}Sn(X) ({LOx}?=aminophenolate ancillary) containing amido ( 1 – 4 ), chloro ( 5 ), or lactyl ( 6 ) coligands (X) promote the ring‐opening polymerization (ROP) of cyclic esters. Complex 6 , which models the first insertion of L ‐lactide, initiates the living ROP of L ‐LA on its own, but the amido derivatives 1 – 4 require the addition of alcohol to do so. Upon addition of one to ten equivalents of iPrOH, precatalysts 1 – 4 promote the ROP of trimethylene carbonate (TMC); yet, hardly any activity is observed if tert‐butyl (R)‐lactate is used instead of iPrOH. Strong inhibition of the reactivity of TMC is also detected for the simultaneous copolymerization of L ‐LA and TMC, or for the block copolymerization of TMC after that of L ‐LA. Experimental and computational data for the {LOx}Sn(OR) complexes (OR=lactyl or lactidyl) replicating the active species during the tin(II)‐mediated ROP of L ‐LA demonstrate that the formation of a five‐membered chelate is largely favored over that of an eight‐membered one, and that it constitutes the resting state of the catalyst during this (co)polymerization. Comprehensive DFT calculations show that, out of the four possible monomer insertion sequences during simultaneous copolymerization of L ‐LA and TMC: 1) TMC then TMC, 2) TMC then L ‐LA, 3) L ‐LA then L ‐LA, and 4) L ‐LA then TMC, the first three are possible. By contrast, insertion of L ‐LA followed by that of TMC (i.e., insertion sequence 4) is endothermic by +1.1 kcal mol?1, which compares unfavorably with consecutive insertions of two L ‐LA units (i.e., insertion sequence 3) (?10.2 kcal mol?1). The copolymerization of L ‐LA and TMC thus proceeds under thermodynamic control. 相似文献
49.
Sarazin Y Liu B Roisnel T Maron L Carpentier JF 《Journal of the American Chemical Society》2011,133(23):9069-9087
Efficient protocols for the syntheses of well-defined, solvent-free cations of the large alkaline-earth (Ae) metals (Ca, Sr, Ba) and their smaller Zn and Mg analogues have been designed. The reaction of 2,4-di-tert-butyl-6-(morpholinomethyl)phenol ({LO(1)}H), 2-{[bis(2-methoxyethyl)amino]methyl}-4,6-di-tert-butylphenol ({LO(2)}H), 2-[(1,4,7,10-tetraoxa-13-azacyclopentadecan-13-yl)methyl]-4,6-di-tert-butylphenol ({LO(3)}H), and 2-[(1,4,7,10-tetraoxa-13-azacyclo-pentadecan-13-yl)methyl]-1,1,1,3,3,3-hexafluoropropan-2-ol ({RO(3)}H) with [H(OEt(2))(2)](+)[H(2)N{B(C(6)F(5))(3)}(2)](-) readily afforded the doubly acidic pro-ligands [{LO(1)}HH](+)[X](-) (1), [{LO(2)}HH](+)[X](-) (2), [{LO(3)}HH](+)[X](-) (3), and [{RO(3)}HH](+)[X](-) (4) ([X](-) = [H(2)N{B(C(6)F(5))(3)}(2)](-)). The addition of 2 to Ca[N(SiMe(3))(2)](2)(THF)(2) and Sr[N(SiMe(3))(2)](2)(THF)(2) yielded [{LO(2)}Ca(THF)(0.5)](+)[X](-) (5) and [{LO(2)}Sr(THF)](+)[X](-) (6), respectively. Alternatively, 5 could also be prepared upon treatment of {LO(2)}CaN(SiMe(3))(2) (7) with [H(OEt(2))(2)](+)[X](-). Complexes [{LO(3)}M](+)[X](-) (M = Zn, 8; Mg, 9; Ca, 10; Sr, 11; Ba, 12) and [{RO(3)}M](+)[X](-) (M = Zn, 13; Mg, 14; Ca, 15; Sr, 16; Ba, 17) were synthesized in high yields (70-90%) by reaction of 3 or 4 with the neutral precursors M[N(SiMe(3))(2)](2)(THF)(x) (M = Zn, Mg, x = 0; M = Ca, Sr, Ba, x = 2). All compounds were fully characterized by spectroscopic methods, and the solid-sate structures of compounds 1, 3, 7, 8, 13, 14, {15}(4)·3CD(2)Cl(2), {16}(4)·3CD(2)Cl(2), and {{17}(4)·EtOH}·3CD(2)Cl(2) were determined by X-ray diffraction crystallography. Whereas the complexes are monomeric in the case of Zn and Mg, they form bimetallic cations in the case of Ca, Sr and Ba; there is no contact between the metal and the weakly coordinating anion. In all metal complexes, the multidentate ligand is κ(6)-coordinated to the metal. Strong intramolecular M···F secondary interactions between the metal and F atoms from the ancillary ligands are observed in the structures of {15}(4)·3CD(2)Cl(2), {16}(4)·3CD(2)Cl(2), and {{17}(4)·EtOH}·3CD(2)Cl(2). VT (19)F{(1)H} NMR provided no direct evidence that these interactions are maintained in solution; nevertheless, significant Ae···F energies of stabilization of 25-26 (Ca, Ba) and 40 kcal·mol(-1) (Sr) were calculated by NBO analysis on DFT-optimized structures. The identity and integrity of the cationic complexes are preserved in solution in the presence of an excess of alcohol (BnOH, (i)PrOH) or L-lactide (L-LA). Efficient binary catalytic systems for the immortal ring-opening polymerization of L-LA (up to 3,000 equiv) are produced upon addition of an excess (5-50 equiv) of external protic nucleophilic agents (BnOH, (i)PrOH) to 8-12 or 13-17. PLLAs with M(n) up to 35,000 g·mol(-1) were produced in a very controlled fashion (M(w)/M(n) ≈ 1.10-1.20) and without epimerization. In each series of catalysts, the following order of catalytic activity was established: Mg ? Zn < Ca < Sr ≈ Ba; also, Ae complexes supported by the aryloxide ligand are more active than their parents supported by the fluorinated alkoxide ancillary, possibly owing to the presence of Ae···F interactions in the latter case. The rate law -d[L-LA]/dt = k(p)·[L-LA](1.0)·[16](1.0)·[BnOH](1.0) was established by NMR kinetic investigations, with the corresponding activation parameters ΔH(++) = 14.8(5) kcal·mol(-1) and ΔS(++) = -7.6(2.0) cal·K(-1)·mol(-1). DFT calculations indicated that the observed order of catalytic activity matches an increase of the L-LA coordination energy onto the cationic metal centers with parallel decrease of the positive metal charge. 相似文献
50.
Abstract— A photoelectrochemical cell has been used to monitor the effects of three enzymes on the photocurrent produced by isolated spinach thylakoids. The enzymes were glucose oxidase, superoxide dismutase and catalase. It is shown that all three inhibit the photocurrent to varying degrees. The results demonstrate that electron transport to the working electrode is mediated by oxygen. Further, the activity monitored originated from photosystem I with oxygen as the acceptor and photosystem II/plastoquinone as the donor. Thus, the photoelectrochemical cell constitutes a potential new approach for the monitoring of pseudocyclic electron transport. 相似文献