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21.
Bonalde I Yanoff BD Salamon MB Van Harlingen DJ Chia EM Mao ZQ Maeno Y 《Physical review letters》2000,85(22):4775-4778
We report measurements of the magnetic penetration depth in single crystals of Sr2RuO4 down to 0.04 K using a tunnel-diode based, self-inductive technique. We observe a power law temperature dependence below 0.8 K, with no sign of a second phase transition nor of a crossover predicted for a multiband superconductor. A power law dependence suggests that the gap function has nodes, inconsistent with candidate p-wave states. We argue that nonlocal effects, rather than impurity scattering, can explain the observed T2 dependence instead of the T-linear behavior expected for line nodes. 相似文献
22.
DJ Smith KW Ledingham RP Singhal T McCanny P Graham HS Kilic P Tzallas C Kosmidis AJ Langley PF Taday 《Rapid communications in mass spectrometry : RCM》1999,13(14):1366-1373
With the development of high intensity femtosecond lasers, the ionisation and dissociation dynamics of molecules has become an area of considerable interest. Using the technique of femtosecond laser mass spectrometry (FLMS), the molecules carbon disulphide, pyrimidine, toluene, cyclohexanone and benzaldehyde are studied with pulse widths of 50 fs in the near infrared (IR) wavelength region (790 nm). Results are presented and contrasted for laser beam intensities around 10(15) and 10(16) W cm(-2). For the lower intensities, the mass spectra yield dominant singly charged parent ions. Additionally, the appearance of doubly charged parent ions is evident for carbon disulphide, toluene and benzaldehyde with envelopes of doubly charged satellite species existing in these local regions. Carbon disulphide also reveals a small triply charged component. Such atomic-like features are thought to be a strong fingerprint of FLMS at these intensities. However, upon increasing the laser intensity to approximately 10(16) W cm(-2), parent ion dominance decreases and the appearance of multiply charged atomic species occurs, particularly carbon. This phenomenon has been attributed to Coulomb explosions in which the fast absorption of many photons may produce transient highly ionised parent species which can subsequently blow apart. Copyright 1999 John Wiley & Sons, Ltd. 相似文献
23.
X Fang KW Ledingham P Graham DJ Smith T McCanny RP Singhal AJ Langley PF Taday 《Rapid communications in mass spectrometry : RCM》1999,13(14):1390-1397
The potential of femtosecond laser time-of-flight mass spectrometry (FLMS) for uniform quantitative analysis of molecules has been investigated. Various samples of molecular gases and vapours have been studied, using ultra-fast ( approximately 50 fs) laser pulses with very high intensity (up to 1.6 x 10(16) Wcm(-2)) for non-resonant multiphoton ionisation/tunnel ionisation. Some of these molecules have high ionisation potentials, requiring up to ten photons for non-resonant ionisation. The relative sensitivity factors (RSF) have been determined as a function of the laser intensity and it has been demonstrated that for molecules with very different masses and ionisation potentials, uniform ionisation has been achieved at the highest laser intensities. Quantitative laser mass spectrometry of molecules is therefore a distinct possibility. Copyright 1999 John Wiley & Sons, Ltd. 相似文献
24.
MR Eskildsen AB Abrahamsen PL Gammel DJ Bishop NH Andersen K Mortensen PC Canfield 《Pramana》2002,58(5-6):903-905
We compare the results of small angle neutron scattering on the flux line lattice (FLL) obtained in the borocarbide superconductor
LuNi2B2C with the applied field along the c- and a-axes. For H‖c the temperature dependence of the FLL structural phase transition from square to hexagonal symmetry was investigated. Above
10 K the transition onset field. H
2(T), rises sharply, bending away from H
c2(T) in contradiction to theoretical predictions of the two merging. For H‖a a first order FLL reorientation transition is observed at H
tr=3–3.5 kOe. Below H
tr the FLL nearest neighbor direction is parallel to the b-axis, and above H
tr to the c-axis. This transition cannot be explained using nonlocal corrections to the London model. 相似文献
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The relative rates of H-transfer between partners in ion-neutral complexes were compared with those in intramolecular rearrangements using results of first differential photoionization mass spectrometry measurements. Complex-mediated H-transfers are inferred to have rates of the same order as those for intramolecular hydrogen rearrangements, suggesting a similar range of motion of the reactive sites in both types of reactions. It is also concluded that at their fastest H-transfers take place between the partners in ion-neutral complexes within at most the time of several rotations of the partners in the complexes. Copyright 1999 John Wiley & Sons, Ltd. 相似文献
28.
Three sharp absorption features in the energy range 2.36–2.55 eV have been detected in the transmission spectrum of Co-diffused ZnSe, and a number of luminescence transitions originating from the lowest of these states at 2.361 eV have been observed. Photoluminescence excitation spectra prove that these are high energy excited states of the Co2+Zn impurity, a conclusion confirmed by comparison of measured and predicted luminescence energies. This represents the first identification of luminescence branching from a higher excited state of a transition metal ion in any semiconductor. The sharp, weakly phonon-coupled transitions involve either intra-impurity excitation or transitions from the impurity to localised states split off from a minimum in the conduction band. The implications of these observations for the mechanism of host-impurity energy transfer and for the nature of the excited state wavefunctions are discussed. 相似文献
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30.
Haifeng Zheng Rui Wang Kan Wang Daniel Wherritt Hadi Arman Michael P. Doyle 《Chemical science》2021,12(13):4819
Brønsted acid catalyzed formal [4 + 4]-, [4 + 3]-, and [4 + 2]-cycloadditions of donor–acceptor cyclobutenes, cyclopropenes, and siloxyalkynes with benzopyrylium ions are reported. [4 + 2]-cyclization/deMayo-type ring-extension cascade processes produce highly functionalized benzocyclooctatrienes, benzocycloheptatrienes, and 2-naphthols in good to excellent yields and selectivities. Moreover, the optical purity of reactant donor–acceptor cyclobutenes is fully retained during the cascade. The 1,3-dicarbonyl product framework of the reaction products provides opportunities for salen-type ligand syntheses and the construction of fused pyrazoles and isoxazoles that reveal a novel rotamer-diastereoisomerism.Brønsted acid catalysis realizes formal [4 + 4]-, [4 + 3]-, and [4 + 2]-cycloadditions of donor–acceptor cyclobutenes, cyclopropanes, and siloxyalkynes with benzopyrylium ions.Medium-sized rings are the core skeletons of many natural products and bioactive molecules,1 and a growing number of strategies have been developed for their synthesis.2 Because of their enthalpic and entropic advantages, ring expansion is a highly efficient methodology for these constructions.3–6 For example, Sun and co-workers have developed acid promoted ring extensions of oxetenium and azetidinium species formed from siloxyalkynes with cyclic acetals and hemiaminals (Scheme 1a).4 Takasu and co-workers have reported an elegant ring expansion with a palladium(ii) catalyzed 4π-electrocyclic ring-opening/Heck arylation cascade with fused cyclobutenes (Scheme 1b).5 Each transformation is initiated by the formation of fused bicyclic units followed by ring expansion or rearrangement to give medium-sized rings.Open in a separate windowScheme 1Cycloaddition/ring expansion background and this work.Strategies for the formation of fused bicyclic compounds rely on cycloaddition of dienes or dipoles with unsaturated cyclic compounds7 and, if the reactant cyclic compound is strained and chiral, the resulting bicyclic compound is activated toward ring opening that results in retention of chirality. We have recently reported access to donor–acceptor cycloalkenes by [3 + n] cycloaddition that have the prerequisites of unsaturated cyclic compounds suitable for cycloaddition.8 Donor–acceptor (D–A) cyclopropenes9 and cyclobutenes10 have sufficient strain in the resulting bicyclic compounds to undergo ring opening. We envision that the selection of a diene or dipolar reactant and suitable reaction conditions could realize cycloaddition and subsequent ring expansion. Benzopyrylium species,11,12 which are generated by metal or acid catalysis, have attracted our attention. We anticipated that their high reactivity would overcome the conventional unfavorable kinetic and/or thermodynamic factors that typically impede medium-sized ring formation. From a mechanistic perspective, benzopyrylium species are often formed by transition metal catalyzed reactions with 2-alkynylbenzaldehydes.11 Recently, the reaction between 1H-isochromene acetal and Brønsted acid catalyst forms the 2-benzopyrylium salts that could react with functional alkenes to give same cycloaddition products.12 Consequently, we believed that the [4 + 2]-cyclization between benzopyrylium species and donor–acceptor cyclobutenes, cyclopropenes, or siloxyalkynes would give bridged oxetenium intermediates, which contain high strain energy that should provide the driving force for ring expansion. The “push and pull” electronic effect of donor–acceptor functional groups facilitates deMayo-type ring-opening of the cyclobutane or cyclopropane skeletons (Scheme 1c).13Here we report bis(trifluoromethanesulfonyl)imide (HNTf2) catalyzed formal [4 + 4]-, [4 + 3]- and [4 + 2]-cycloaddition reactions of D–A cyclobutenes, cyclopropenes, and siloxyalkynes with benzopyrylium salts. Polysubstituted benzo-cyclooctatrienes, benzocycloheptatrienes and 2-naphthols, are produced in good to excellent yields and selectivities. Complete retention of configuration occurs using chiral cyclobutenes, and opportunities for further functionalization are built into these constructions.Initially, we conducted transition metal catalyzed reactions with 2-alkynylbenzaldehyde intending to produce the corresponding benzopyrylium ion and explore the possibility of cycloaddition/ring opening with donor–acceptor cyclobutene 2a. Use of Ph3PAuCl/AgSbF6, Pd(OAc)2 and Cu(OTf)2, which were efficient catalysts in previous transformations,11 gave only a trace amount of cycloaddition product (Fig. 1). Spectral analysis showed that mostly starting material remained (Fig. 1-i and ii). Increasing the reaction temperature led only to decomposition of 2-alkynylbenzaldehyde (Fig. 1-iv) or donor–acceptor cyclobutene 2a (Fig. 1-iv).Open in a separate windowFig. 1Reaction of 2-alkynylbenzaldehyde with donor–acceptor cyclobutene 2a.From these disappointments we turned our attention to 1H-isochromene acetal 1a as the benzopyrylium ion precursor. Various Lewis acid catalysts were employed with limited success, but we were pleased to observe the formation of the desired formal [4 + 4]-cycloaddition benzocyclooctatriene product 3aa, albeit in low yields (Table 1, entries 1–6). Selection of the Brønsted super acid HNTf2 (ref. 14) proved to be the most promising, producing 3aa in 40% yield (Table 1, entry 7). Increasing the amount of D–A cyclobutene 2a by 30% gave a much higher yield of 3aa (Table 1, entry 8 vs. 7). Optimization of the stoichiometric reaction between 1a and 2a by increasing the reaction temperature from rt to 35 °C led to the formation of the desired product in 76% isolated yield (Table 1, entry 9 vs. 8). However, a further increase in the reaction temperature (Table 1, entry 10) or reducing the catalyst loading to 5 mol% did not improve the yield of 3aa (Table 1, entry 11).Optimization of reaction conditionsa
Open in a separate windowaReactions were performed by adding the catalyst (10 mol%) to 1a (0.1 mmol) and 2a (0.1 mmol) in CH2Cl2 (2 mL) at the corresponding temperature for 24 h.bYields were determined by 1H NMR spectroscopic analysis with CH2Br2 as the internal standard.c1.3 equiv. 2a was used.dIsolated yield.eReaction performed at 60 °C for 12 h.f5 mol% catalyst loading.With optimized conditions using 1a in hand, we examined the scope of the formal [4 + 4]-cycloaddition reactions of D–A cyclobutenes 2 with a diverse set of acetal compounds 1. As shown in Scheme 2, a wide range of acetal substrates (1a–1i) with different substituents at different positions all reacted smoothly with D–A cyclobutene 2a to form the corresponding benzocyclooctatriene products 3 in good to excellent yields. Structural variations in the acetals produced only modest changes in product yields which ranged from 55 to 87%. Similarly, both electron-withdrawing and electron-donating substituents at the 4-position of the cyclobutene phenyl ring produced the corresponding products (3db–3dd) in good yields, and 2-naphthyl (2e) and 2-thienyl (2f) substituted cyclobutenes were suitable substrates (85% and 51% product yields, respectively). trans-1,2,3,4-Tetrasubstituted (R2 = CH3) 2-sil-oxycyclobutenecarboxylate 2g also underwent [4 + 4]-cycloaddition with 1d in good yield and fully retained its diastereoselectivity. The structure of 3fa was confirmed by X-ray diffraction (Scheme 2).15Open in a separate windowScheme 2Scope of the [4 + 4]-cycloaddition reaction of D–A cyclobutenes and 1H-isochromene acetals.a aReactions were performed by adding HNTf2 (10 mol%) to 1 (0.1 mmol) and 2 (0.13 mmol) in CH2Cl2 (2 mL) at 35 °C for 24 h. Isolated yields are reported.Chiral donor–acceptor cyclobutenes with high enantiomeric excess and diastereoselectivity are conveniently obtained by catalytic [3 + 1]-cycloaddition of enoldiazoacetates with acyl ylides of sulfur.10 To determine if optical purity is retained, chiral D–A cyclobutene 2a (80% ee) was reacted with 1d under the optimized conditions, and the corresponding benzocyclo-octatriene product 3da was obtained in good yield with complete retention of configuration (Scheme 3, eqn (1)). With trans-disubstituted 2g and 2h that have higher optical purity, however, 3dg and 3dh were obtained in moderate yields with full retention of diastereo- and enantioselectivities, but addition products 8dg and 8dh were formed competitively (Scheme 3, eqn (2)). These compounds resulted from initial addition then desilylation, indicating that the [4 + 2]-cyclization is a stepwise reaction. Attempts to suppress the competing pathway by changing solvents or using the isopropyl acetal substrate to form a bulky 2-propanol nucleophile (1j) failed (for details, see ESI†). However, p-methoxy (R1) substituted 1g that would stabilize the incipient benzopyrylium ion gave higher selectivity (4 : 1 vs. 2 : 1), and the desired [4 + 4] cycloaddition product 3gg was isolated in 50% yield with 97% ee and >19 : 1 dr (Scheme 3, eqn (3)).Open in a separate windowScheme 3Stereochemical features of the [4 + 4]-cycloaddition of D–A cyclobutenes and 1H-isochromene acetals.a aReactions were performed by adding HNTf2 (10 mol%) to 1 (0.1 mmol) and 2 (0.13 mmol) in CH2Cl2 (2 mL) at 35 °C for 24 h. Isolated yields are reported.To further expand the generality of this strategy, we investigated its use with donor–acceptor cyclopropenes 4. The desired formal [4 + 3]-cycloaddition products 5 were obtained in good to excellent yields (Scheme 4). Optimized conditions used 20 mol% HNTf2 catalyst with 4 Å molecular sieves at room temperature for 2 h. The scope of this [4 + 3]-cycloaddition reaction with cyclopropenes 4 showed that acetals bearing both electron-donating and electron-withdrawing substituents on the aromatic ring were tolerated. However, as with [4 + 4]-cycloaddition reactions, the [4 + 3] reactions of 1 with R1 = alkyl or H did not produce any of the desired products. Furthermore, 3-substituted cyclopropenes 4b–4d participated in this reaction, and their products (5ab–5ad) were obtained in 63%–81% yields.Open in a separate windowScheme 4Scope of the [4 + 3]-cycloaddition reaction of D–A cyclopropenes and 1H-isochromene acetals.a aReactions were performed by adding HNTf2 (20 mol%) to 1 (0.2 mmol), 4 (0.24 mmol) and 4 Å (50 mg) in CH2Cl2 (2 mL) at rt for 2 h. Isolated yields are reported.Siloxyalkynes 6, as electron-rich alkynes, have been widely used in diverse cyclization reaction.4,16 We expected that 6 could also participate in [4 + 2]-cyclization/ring-expansion cascade processes, giving substituted 2-naphthol products. Interestingly, substituent controlled diverse products were obtained in good to excellent reactivity and selectivity (Scheme 5). Aryl (R1) substituted acetals (1a–1d, 1f, 1h, 1i) reacted with siloxyalkynes 6a–6d, giving 2-naphthols (7aa–7ad and 7ba–7ia) in 35%–96% yields. With electron-donating group (EDG) substituents (7ba and 7ca) on the aromatic ring, higher reactivity was observed relative to those with electron-withdrawing groups (7da–7ia). In addition, the acetal with R1 = H (1m) reacted with siloxyalkynes 6 to form the 2-naphthol-1-carboxaldehyde derivative in good yield, and the structure of 7ma was confirmed by X-ray diffraction (Scheme 5b).15 Intriguingly, the n-butyl (R1) substituted acetal 1n reacted with siloxyalkynes via a [4 + 2]-cyclization with loss of methyl pentanoate (BuCO2CH3), affording siloxy naphthalenes 7na–7nd that are important precursors to the widely used axially chiral 2,2′-binols.17 The substrate scope of siloxyalkynes 6 for their formal [4 + 2]-cycloaddition reaction with n-butyl substituted acetal 1n was also explored (Scheme 5c). In all cases methyl pentanoate was eliminated to form 2,3-disubstituted naphthalene products (7na–7nd). Alkyl substituted siloxyalkynes (6a–6c) showed higher reactivity compared with phenyl substituted siloxyalkynes 6d. It should be mentioned that, recently, a similar transformation using BF3·OEt2 as catalyst or in excess (2 equiv.) with 2,4,6-collidine (1 equiv.) was reported,18 and HNTf2 was stated to be much less effective. To clarify this discrepancy, we carefully repeated these transformations (7ma and 7na) and found that all starting materials are completely consumed in less than 10 min to deliver [4 + 2]-cycloaddition products in good yields. Prolonging the reaction time to 12 hours, which was the reaction time used by the authors, results in their decomposition to a complex mixture of materials.Open in a separate windowScheme 5Scope of the [4 + 2]-cycloaddition reaction of siloxyalkynes and 1H-isochromene acetals.a aReactions were performed by adding HNTf2 (10–30 mol%) to 1 (0.2 mmol) and 6 (0.3–0.4 mmol) in CH2Cl2 (2 mL) at rt for 10 min. Isolated yields are reported. b40 mol% HNTf2 catalyst was used.To illustrate the utility of this process, a large scale catalytic [4 + 4] cycloaddition was performed, and adduct 3da was obtained in 87% yield. Further transformations were conducted for the synthesis of pyrazole and isoxazole structures based on its 1,3-dicarbonyl skeleton (Fig. 2a). Compound 3da reacted with hydrazine and hydroxylamine in refluxed ethanol, affording pyrazole 14da and isoxazole 15da in 89% yield or 66% yield, respectively. The structure of 15da was confirmed by X-ray diffraction.15 Interestingly, two NMR distinguishable interconvertible diastereoisomers were detected for each of these eight-membered cyclic products (2.5 : 1 and 5 : 1 dr for 14da and 15da, respectively, in CDCl3). These diastereoisomers are rotamers (for details, see ESI†) that exist at equilibrium with each other in solution but form one crystalline product (X-ray structure of 15da). In addition, the cycloaddition product 7ma reacted with chiral 1,2-cyclohexanediamine and 1,2-diphenylethylenediamine to give salen-type ligands L1 and L2 in 53% yield and 74% yield, respectively, which provides new opportunities for ligand screening (Fig. 2b).19Open in a separate windowFig. 2Large scale reaction, further transformations, and ligands synthesis.In the mechanistic possibility considered for these HNTf2 catalyzed cycloaddition reactions (Fig. 3), protonation of acetal 1 with HNTf2 gives the corresponding highly reactive benzopyrylium intermediate int-I, which reacts with donor–acceptor cyclobutenes 2, cyclopropenes 4, or siloxyalkynes 6 affording addition intermediates int-II that undergo ring closure to int-III. Ring expansion then occurs to deliver 3, 5 and 7 in good to excellent yields with fully retained stereoselectivities. Furthermore, the formed TIPSNTf2 ([4 + 4]- and [4 + 3]-cycloaddition) or HNTf2 {[4 + 2] cycloaddition} are active acid catalysts for the conversion of 1 to benzopyrylium intermediate int-I that continues the catalytic cycle. With sterically larger D–A cyclobutenes or when a less ring-strained benzocyclopentene 12 is employed (for details, see ESI†), the competing direct desilylation of int-II occurs, delivering addition byproducts 8 or 13. Compounds 7na–7nd arise from the analog to int-III from which ketene formation or methanol displacement effects 1,4-elimination.Open in a separate windowFig. 3Proposed mechanism. 相似文献
| Entry | Cat (10 mol%) | Temp. (°C) | Yieldb |
|---|---|---|---|
| 1 | Sc(OTf)3 | rt | 23 |
| 2 | Yb(OTf)3 | rt | Trace |
| 3 | In(OTf)3 | rt | 16 |
| 4 | TiCl4 | rt | Trace |
| 5 | BF3·OEt2 | rt | 20 |
| 6 | TMSOTf | rt | 17 |
| 7 | HNTf2 | rt | 40 |
| 8c | HNTf2 | rt | 67 |
| 9c | HNTf2 | 35 | 78(76)d |
| 10c,e | HNTf2 | 60 | 62 |
| 11c,f | HNTf2 | 35 | 50 |