In this work, the encapsulations of halide ions including F?, Cl?, and Br? by cyclic peptide nanocapsule as ion carrier (F?, Cl?, and Br? @(Ala4...Ala4)) were investigated using the dispersion corrected density functional theory (DFT) employing CAM-B3LYP functional and the 6–311?+?G (d, p) basis set in the gas phase. The electronic binding energy (Ebind), binding enthalpy (Hbind), and binding Gibbs free energy (Gbind) for each anion were calculated and showed that the stability order of the complexes based on their calculated Ebind is F??>?Cl??>?Br? @(Ala4...Ala4). The calculated value of Gbind for F? @(Ala4...Ala4) was ??29.77 kcal/mol showing the formation of this complex is thermodynamically favorable while the formation of Br? @(Ala4...Ala4) is 14.35 kcal/mol which shows that the encapsulation of Br? is not possible. The calculated value of Gbind for Cl? @(Ala4...Ala4) was ??0.57 kcal/mol which shows that Cl? ion can be reversibly stored inside the nanocapsule. The NBO analysis was also performed to investigate the charge transfer between two cyclic peptides in the complexes and also between the anion and the nanocapsule. The NBO analysis showed that the strongest hydrogen bonds between two cyclic peptides are in the complex. 相似文献
Reaction pathways of ethylene and carbon monoxide on the singlet and triplet potential energy surfaces (PESs) have been calculated at B3LYP/6-311++G (3df, 3dp), G3B3 and CCSD(T)//B3LYP levels. Reaction mechanisms have been investigated by analysis of various structures. Suggested reaction mechanisms reveal that 3P3(CH2CHCHO) and 3P4(CH3CCHO) are thermodynamically stable adducts with the negative value in Gibbs free energies on the triplet PES. In addition, results show that one intersystem crossing exists between triplet and singlet PESs, which are obtained by scanning of the C–C bond length in 1IN3 and 3IN7 species. 相似文献
The reaction mechanism of C2H2 and N2O on the singlet potential energy surface is investigated in this study, at the B3LYP/6-311++G(3df,3pd), MP2/6-311++G(d,p), and CCSD(T) levels of theory. We have obtained three kinds of products in both methods, B3LYP and MP2, which have enough thermodynamic stability. The results reveal that the product P1, CH2CO + N2, is spontaneous and exothermic with ?86.176 and ?83.149 kcal/mol in Gibbs free energy and enthalpy of reaction at the MP2 level, respectively. Hence, the product P1 is thermodynamically the most favored adduct of the C2H2 + N2O gas phase reaction at atmospheric pressure and 298.15 K temperature. 相似文献
We report a photochemically induced, hydroxy-directed fluorination that addresses the prevailing challenge of high diastereoselectivity in this burgeoning field. Numerous simple and complex motifs showcase a spectrum of regio- and stereochemical outcomes based on the configuration of the hydroxy group. Notable examples include a long-sought switch in the selectivity of the refractory sclareolide core, an override of benzylic fluorination, and a rare case of 3,3′-difluorination. Furthermore, calculations illuminate a low barrier transition state for fluorination, supporting our notion that alcohols are engaged in coordinated reagent direction. A hydrogen bonding interaction between the innate hydroxy directing group and fluorine is also highlighted for several substrates with 19F–1H HOESY experiments, calculations, and more. We report a photochemical, hydroxy-directed fluorination that addresses the prevailing challenge of high diastereoselectivity. Numerous motifs showcase a range of regio- and stereochemical outcomes based on the configuration of the hydroxy group.The hydroxy (OH) group is treasured and versatile in chemistry and biology.1 Its ubiquity in nature and broad spectrum of chemical properties make it an attractive source as a potential directing group.2 The exploitation of the mild Lewis basicity exhibited by alcohols has afforded several elegant pathways for selective functionalization (e.g., Sharpless epoxidation,3 homogeneous hydrogenation,4 cross-coupling reactions,5 among others6). Recently, we reported a photochemically promoted carbonyl-directed aliphatic fluorination, and most notably, established the key role that C–H⋯O hydrogen bonds play in the success of the reaction.7 Our detailed mechanistic investigations prompt us to postulate that other Lewis basic functional groups (such as –OH) can direct fluorination in highly complementary ways.8 In this communication, we report a hydroxy-directed aliphatic fluorination method that exhibits unique directing properties and greatly expands the domain of radical fluorination into the less established realm governing high diastereoselectivity.9Our first inclination that functional groups other than carbonyls may influence fluorination regiochemical outcomes was obtained while screening substrates for our published ketone-directed radical-based method (Scheme 1).8a In this example, we surmised that oxidation of the tertiary hydroxy group on substrate 1 cannot occur and would demonstrate functional group tolerance (directing to C11, compound 2). Surprisingly, the two major regioisomers (products 3 and 4) are derivatized by Selectfluor (SF) on C12 and C16 – indicative of the freely rotating hydroxyl directing fluorination. Without an obvious explanation of how these groups could be involved in dictating regiochemistry, we continued the mechanistic study of carbonyl-directed fluorination (Scheme 2A). We established that the regioselective coordinated hydrogen atom abstraction occurs by hydrogen bonding between a strategically placed carbonyl and Selectfluor radical dication (SRD).7 However, we noted that the subsequent radical fluorination is not diastereoselective due to the locally planar nature of carbonyl groups. Thus, we posed the question: are there other directing groups that can provide both regio- and diastereoselectivity? Such a group would optimally be attached to a sp3 hybridized carbon; thus the “three dimensional” hydroxy carbon logically comes to mind as an attractive choice, and Scheme 1 illustrates the first positive hint.Open in a separate windowScheme 1Observed products for the fluorination of compound 1.Open in a separate windowScheme 2(A) Proposed mechanism, (B) β-caryophyllene alcohol hypochlorite derivative synthetic probe, (C) isodesmic relation of transition states showing the general importance of the hydroxy group to reactivity (ωB97xd/6-31+G*), and (D) 1H NMR experiment with Selectfluor and various additives at different concentrations.We began our detailed study with a simple substrate that contains a tertiary hydroxyl group. Alcohol 5 was synthesized stereoselectively by the reaction of 3-methylcyclohexanone, FeCl3, and 4-chlorophenylmagnesium bromide;10 the 4-chlorophenyl substituent allows for an uncomplicated product identification and isolation (aromatic chromophore). We sought to determine optimal reaction conditions by examination of numerous photosensitizers, bases, solvents, and light sources (7 Although we utilize cool blue LEDs (sharp cutoff ca. 400 nm), CFLs (small amount of UVB (280–315 nm) and UVA (315–400 nm)) are useable as well.11 A mild base additive was also found to neutralize adventitious HF and improve yields in the substrates indicated (
Open in a separate windowaUnless stated otherwise: substrate (0.25 mmol, 1.0 equiv.), Selectfluor (0.50 mmol, 2.0 equiv.), NaHCO3 (0.25 mmol, 1.0 equiv.), and sensitizer (0.025 mmol, 10 mol%) were dissolved in MeCN (4.0 mL) and irradiated with cool white LEDs for 14 h.Substrate scopea
Open in a separate windowaUnless otherwise specified, the substrate (0.25 mmol, 1.0 equiv.), Selectfluor (0.50 mmol, 2.0 equiv.), NaHCO3 (0.25 mmol, 1.0 equiv. or 0.0 equiv.), and benzil (0.025 mmol 10 mol%) were stirred in MeCN (4.0 mL) and irradiated with cool white LEDs for 14 h. Yields were determined by integration of 19F NMR signals relative to an internal standard and confirmed by isolation of products through column chromatography on silica gel. Yields based on recovered starting material in parentheses. Major diastereomer (with respect to C–F bond) depicted where known.b1.2 equiv. of Selectfluor used.c1.0 equiv. of NaHCO3.d0.0 equiv. of NaHCO3.e3.0 equiv. of Selectfluor used.fIncluding the monofluoride (approx. 11%) with starting material.The screening concurrently buttresses our claim that hydroxy-directed fluorination is proceeding through a mechanism involving a network of C–H⋯OH hydrogen bonds.12 Other N–F reagents (for example, N-fluorobenzenesulfonimide and N-fluoropyridinium tetrafluoroborate) do not provide the desired fluorinated product 6. The 1,3-diaxial relationship shown in Fig. 1 presents an intramolecular competition: tertiary vs. secondary C–H abstraction (O⋯H–C calculated distances: 2.62 and 2.70 Å at B3LYP 6-311++G**, respectively). The tertiary fluoride is the major product in this case.Open in a separate windowFig. 1Example of an intramolecular competition (secondary vs. tertiary C–H abstraction/fluorination) and calculated C–H⋯O distances of compound 5 (B3LYP/6-311++G**).With optimized conditions established, we assessed the site-selectivity of the method with a molecule derived from the acid catalyzed cyclization of α-caryophyllene, β-caryophyllene alcohol (commonly used as a fragrance ingredient in cosmetics, soaps, and detergents).13 When subjected to fluorination conditions, it targets the strained cyclobutane ring (substrate 7) in 52% yield (14 The hydroxy group stereochemistry is poised to direct fluorination to either the C8 or C10 positions (compound 9) due to the plane of symmetry (Fig. 3A). Moreover, we synthesized a complementary derivative through PCC oxidation followed by a Grignard reaction, thereby switching directionality of the hydroxy group (Fig. 3A) to target the C3 or C5 positions instead (compound 8). We found the resultant fluorinated products to be what one expects if engaged in coordinated hydrogen atom transfer (HAT) (55% and 40% for molecules 9 and 8) – a change in regiochemistry based on the stereochemistry of the alcohol. Additionally, only a single stereoisomer is produced for both (d.r. 99 : 1) and reinforce this study as a salient example of diastereoselective radical fluorination.Open in a separate windowFig. 3Examples of hydroxy group stereochemical switches.In the midst of characterizing compound 9, we uncovered a noteworthy hydrogen bonding interaction. Firstly, our plan was to identify the –OH peak within the 1H NMR spectrum and determine if there is a through-space interaction with fluorine in the 19F–1H HOESY NMR spectrum (ultimately aiding in assigning the stereochemistry of the fluorine).15 At first glance, no peaks were immediately discernible as the –OH; however, when a stoichiometric amount of H2O is added, it becomes apparent that the –OH group and geminal proton to the hydroxy peaks broaden by rapid proton exchange (Fig. 2A). Upon closer examination of the dry 1H NMR spectrum, the –OH peak appears to be a sharp doublet of doublets: one bond coupling to the geminal C–H proton of 9 Hz and one of the largest reported through-space couplings to fluorine of 20 Hz. The 19F–1H HOESY spectrum also supports our regio- and stereochemical assignment – a strong interaction between fluorine and Ha, Hb, and Hd, as well as no apparent interaction with Hc and He (Fig. 2B). Consequently, we postulate that intramolecular hydrogen bonding is responsible for the considerable coupling constant. This conclusion is also supported by calculations at B3LYP/6-311++G** (Fig. 2C): the O–H–F angle is given as 140° and F⋯H–O bond distance is 1.97 Å.Open in a separate windowFig. 2(A) Top spectrum (pink) has broadened peaks due to adventitious H2O in solution. (B) Strong interaction observed between the installed fluorine and designated hydroxy proton in the 19F–1H HOESY NMR spectrum. (C) Calculated structure for compound 9 at B3LYP/6-311++G* revealing the hydroxy proton aiming toward the fluorine.Appreciating the complexity and biological significance of steroids,16 we derivatized dehydroepiandrosterone to afford fluorinated substrate 10 (42%; d.r. 99 : 1). Computational modeling assisted in verifying that the β-hydroxy group targets the C12 position (B3LYP/6-311++G**); furthermore, the β-fluoro isomer is the major product (validated by NOESY, 1H, and 19F NMR). Additionally, we subjected 17α-hydroxyprogesterone (endogenous progestogen steroid hormone17) to fluorination conditions and found the α-fluoro product (11) as the major diastereomer in 55% yield (99 : 1 d.r.). To investigate further the notion of coordinated fluorination and explanation of the observed stereoisomers (e.g., β-hydroxy/β-fluoro and α-hydroxy/α-fluoro), we calculated a simplified system comparing the fluorination of 1-propyl radical and γ-propanol radical (Scheme 2C). The reaction can be distilled into two key steps: a site-selective HAT, followed by a diastereoselective fluorination reaction. The following isodesmic relation (ωB97xd/6-31+G*, −7.63 kcal mol−1) illustrates the stabilizing energetic role that the hydroxy group plays in commanding diastereoselectivity. The transition states represent low barrier processes; a solvent dielectric was necessary to find saddle points.Additionally, a simple Protein Data Bank (PDB) survey showed numerous intermolecular close contacts between hydroxy groups and H–C–+NR3 moieties.18 What is more, solutions of Selectfluor with various alcohols at different concentrations reveal characteristic H–C–+NR3 downfield chemical shifts in the 1H NMR spectra (Scheme 2D).19 Both of these observations buttress the claim of a putative hydrogen bonding interaction between Selectfluor and the hydroxy group.We theorize that the regioselective HAT step proceeds similarly to the reported carbonyl-directed pathway (Scheme 2A) involving Selectfluor radical cation coordination (considering the likenesses in conditions and aforementioned Lewis basicity logic). Alternatively, one can imagine the reaction proceeding through a Barton20 or Hofmann–Löffler–Freytag21 style mechanism. To probe this possibility, we employed a β-caryophyllene alcohol hypochlorite derivative to form the alkoxy radical directly, and found that under standard conditions there is complex fragmentation and nonselective fluorination (Scheme 2B). Lastly, we compared the hydroxy versus carbonyl group SF coordination computationally. The carbonyl group is preferred to bind to SF through nonclassical C–H⋯O hydrogen bonds preferentially over the hydroxy group, as the following isodesmic relation shows (acetone and t-BuOH as models; ωB97xd/6-31+G*, −3.81 kcal mol−1), but, once again, rigidity and propinquity are ultimately more important factors in determining directing effects (Scheme 3).Open in a separate windowScheme 3Isodesmic equation comparing carbonyl versus hydroxy group Selectfluor coordination.The tetrahedral nature of hydroxy groups provides unique access to previously unobtainable sites. For example, we compared menthol and an alkylated congener to form products 12 and 13 (Fig. 3B). The hydroxy group in the precursor to 12 is in the equatorial position, mandating the exocyclic isopropyl group as the reactive site (40% yield).22 In the precursor to 13, the methyl and isopropyl substituent lock the hydroxy group into the axial position, targeting its endocyclic tertiary site through a 1,3-diaxial relationship to afford fluorinated product in 57% yield (d.r. 99 : 1). In all, the comparison showcases the versatility in directing ability, offering a choice of regio- and stereoselectivity based on the stereochemistry of the hydroxy group. The directing system only necessitates two features based on our results: (1) the hydroxy group must be either secondary or tertiary (primary tends to favor oxidation) and (2) the oxygen atom must be within the range of 2.4–3.2 Å of the targeted secondary or tertiary hydrogen.Among the several biologically active compounds we screened, caratol derivatives 14 and 15 were found to be attractive candidates that reveal directed fluorination to an exocyclic isopropyl group (23).24 After extraction, isolation, and derivatization, molecules 14 and 15 are afforded in 65% and 83% yield (25 Groves,9f Britton,26 and others.27 The derived alcohol finally overrode this natural tendency and directed to the predicted position in 56% (d.r. 99 : 1) (product 16). Smaller amounts of competitive polar effect fluorination were observed at the C2 and C3 positions, highlighting how challenging a problem the functionalization of the sclareolide core presents.28,29An altered dihydroactinidiolide was found to participate in the fluorination through a 1,3-diaxial guided HAT and fluorination in 55% yield (product 17, d.r. 99 : 1). We next modeled several more substrates that participated in similar 1,3 relationships; however, each exhibited a variation from one another (e.g., ring size or fused aromatic ring). Products 19 and 18 displayed the reaction''s capability to direct to the desired positions with an expanded (65%; d.r. 99 : 1) and reduced (45%; d.r. 99 : 1) ring system when compared to the previous 6-membered ring examples. Additionally, we examined a methylated α-tetralone derivative. The desired 3-fluoro product 20 forms in 43% yield (d.r. 99 : 1), overriding benzylic fluorination (Scheme 4).30 Under identical conditions α-tetralone provides 4-fluorotetralone in 48% yield. In similar motif, 1-phenylindanol, we intentionally targeted the benzylic position in a 90% and 10 : 1 d.r. (product 21). Unlike the methylated α-tetralone derivative, the geometry of the starting material calculated at B3LYP/6-311++G** shows the hydroxy group is not truly axial and is 4.30 Å from the targeted C–H bond, explaining the dip in diastereoselectivity.Open in a separate windowScheme 4Comparing fluorination outcomes for different functional groups.Next, we examined an isomer of borneol that is widely used in perfumery, fenchol.31 The secondary alcohol displays a diastereoselective fluorination in 38% (d.r. 99 : 1) (product 22). Our last designed motif was ideally constructed to have a doubly-directing effect. Our observations show that a well-positioned hydroxy group not only provides sequential regioselective hydrogen atom abstraction but also displays a powerful demonstration of Selectfluor guidance to afford the cis-difluoro product (23) in 33% yield (85% brsm, d.r. 99 : 1). Spectroscopically (1H, 13C, and 19F NMR), the product possesses apparent Cs symmetry and showcases close interactions (e.g., diagnostic couplings and chemical shifts). cis-Polyfluorocycloalkanes are of intense current interest in materials chemistry, wherein faces of differing polarity can complement one another.32All in all, this photochemical hydroxy-directed fluorination report represents one of the first steps in commanding diastereoselectivity within the field of radical fluorination. An ability to dictate regio- and stereoselectivity is demonstrated in a variety of substrates by simply switching the stereochemistry of the hydroxy group. Computations support the key role of Selectfluor coordination to the key hydroxy group in the fluorination step. Future studies will seek to uncover other compatible Lewis basic functional groups, expanding further the versatility of radical fluorination. 相似文献
We report on transport measurements of the insulating state that forms at the charge neutrality point of graphene in a magnetic field. Using both conventional two-terminal measurements, sensitive to bulk and edge conductance, and Corbino measurements, sensitive only to the bulk conductance, we observed a vanishing conductance with increasing magnetic fields. By examining the resistance changes of this insulating state with varying perpendicular and in-plane fields, we probe the spin-active components of the excitations in total fields of up to 45?T. Our results indicate that the ν=0 quantum Hall state in single layer graphene is not spin-polarized. 相似文献
The magnetic biocompatible rod-like ZnS/CuFe2O4/agar organometallic hybrid catalyst was designed and prepared based on a natural macromolecule (agar) through a green and convenient method using inexpensive, nontoxic, and easily available substances. Then, the as-prepared catalyst was characterized by several techniques such as Fourier transform-infrared spectroscopy, energy-dispersive X-ray analysis, scanning electron microscopy image, transmission electron microscopy, vibrating sample magnetometry curve, X-ray diffraction pattern, and thermogravimetric analysis. Eventually, the catalytic application of the ZnS/CuFe2O4/agar nanobiocomposite was assessed in sequential Knoevenagel condensation–Michael addition reaction of dimedone, malononitrile, and different substituted aromatic aldehydes for the synthesis of 2-amino-tetrahydro-4H-chromene-3-carbonitrile derivatives. Some notable strengths of this environmentally benign catalyst include simplicity of catalyst preparation and separation, affording desired products with satisfactory yields (81%–97%) in very short reaction times (3–18 min), and with no need for complicated work-up processes. Experimental tests showed that the catalyst can be successfully reused after five sequential runs without significant reduction in its catalytic efficiency. 相似文献
We report on magnetotransport measurements of multiterminal suspended graphene devices. Fully developed integer quantum Hall states appear in magnetic fields as low as 2 T. At higher fields the formation of longitudinal resistance minima and transverse resistance plateaus are seen corresponding to fractional quantum Hall states, most strongly for ν=1/3. By measuring the temperature dependence of these resistance minima, the energy gap for the 1/3 fractional state in graphene is determined to be at ～20 K at 14 T. 相似文献
