Lewis Base Functional Groups Research Articles

Cobalt-Catalyzed Regio- and Enantioselective Hydroalkylation of 1,1-Disubstituted Styrenes

AbstractThe metal hydride catalyzed alkene hydroalkylation enables efficient alkyl–alkyl coupling, yielding structurally diverse chiral organic compounds. However, the control of stereochemical selectivity in alkene hydroalkylation still heavily relies on the assistance of substrate Lewis basic functional groups or polar heteroatom functional groups. We have recently developed a cobalt hydride catalytic system and established a paradigm of enantioselective control assisted by C–H···π noncovalent interactions. This approach enables the asymmetric hydroalkylation of 1,1-disubstituted styrenes, thereby circumventing the limitations imposed by substrate heteroatom functional groups.1 Introduction2 Reaction Development3 Synthetic Applications4 Mechanistic Investigation5 Conclusion and Future Outlook

Structure Activity Relationships for Second‐Coordination Sphere Functional Group Dependent CO2 Reduction by Manganese Bipyridyl Electrocatalysts

AbstractA series of twelve second coordination sphere (SCS) functionalized manganese tricarbonyl bipyridyl complexes are investigated for their electrocatalytic CO2 reduction properties in acetonitrile. A qualitative and quantitative assessment of the SCS functional groups is discussed with respect to the catalysts’ thermodynamic and kinetic efficiencies, and their product selectivities. In probing a broad scope of functional groups, it is clear that only the aprotic ortho‐arylester SCS is capable of promoting the highly desired low‐overpotential proton‐transfer electron‐transfer (PT‐ET) pathway for selective CO production. The ortho‐phenolic analogues cause an increase in overpotential with a product selectivity favoring H2 evolution, consistent with a high‐overpotential pathway via the anionic [Mn−H]− intermediate. Alternative aprotic Lewis base functional groups such as trifluoromethyl, morpholine and acetamide are shown to also be capable of intermediate manganese hydride generation. The tertiary amine substituent, 2‐morpholinophenyl, exhibits a desirable product distribution characteristic of syn‐gas (CO : H2=30 : 48) with an impressive turnover frequency, while the secondary amine group, 2‐acetamidophenyl, induces a notable shift in selectivity with a faradaic yield of 55 % for the formate (HCO2−) product. In addition to their catalytic properties, cyclic voltammetry and infrared spectroelectrochemistry (IR‐SEC) studies are presented to probe pre‐catalyst electronic properties and the two‐electron reduction activation pathway.

Site-Selective Palladium-catalyzed Oxidation of Unprotected Aminoglycosides and Sugar Phosphates.

The site-selective modification of complex biomolecules by transition metal-catalysis is highly warranted, but often thwarted by the presence of Lewis basic functional groups. This study demonstrates that protonation of amines and phosphates in carbohydrates circumvents catalyst inhibition in palladium-catalyzed site-selective oxidation. Both aminoglycosides and sugar phosphates, compound classes that up till now largely escaped direct modification, are oxidized with good efficiency. Site-selective oxidation of kanamycin and amikacin was used to prepare a set of 3'-modified aminoglycoside derivatives of which two showed promising activity against antibiotic-resistant E. coli strains.

Ruthenium-Catalyzed Aminocarbonylation with Isocyanates Through Weak Coordinating Groups.

Introducing amide functional groups under mild conditions has growing importance owing to the prevalence of such moiety in biologically active molecules. Herein, we disclose a mild protocol for the directed ruthenium-catalyzed C-H aminocarbonylation with isocyanates as the amidating agents developed through high-throughput experimentation (HTE). The redox-neutral and base-free reaction is guided by weakly Lewis basic functional groups, including anilides, lactams and carbamates to access anthranilamide derivatives. The synthetic utility of this transformation is reflected by large-scale synthesis and late-stage functionalization.

Azetidine synthesis by La(OTf)3-catalyzed intramolecular regioselective aminolysis of cis-3,4-epoxy amines.

Azetidine is a prevalent structural motif found in various biologically active compounds. In this research paper, we report La(OTf)3-catalyzed intramolecular regioselective aminolysis of cis-3,4-epoxy amines to afford azetidines. This reaction proceeded in high yields even in the presence of acid-sensitive and Lewis basic functional groups.

Synergistic Effects of Lewis Acid-Base Pair Sites─Hf-MOFs with Functional Groups as Distinguished Catalysts for the Cycloaddition of Epoxides with CO2.

The incorporation of Lewis acid-base sites in catalysts has been considered as a significant approach to fabricating bifunctional catalysts with efficient catalytic activity for CO2 fixation. In this paper, a series of Hafnium-based metal-organic frameworks (Hf-MOFs), NU-912(Hf) and NU-912-X(Hf)-X (X = -NH2, -Br, -CN, and -I) derivatives assembled by Lewis acidic Hf6(μ3-O)4(μ3-OH)4(H2O)4(OH)4 (Hf6) clusters and Lewis base-attached organic linkers, are successfully synthesized by a facile ligand functionalization method. These isostructural Hf-MOFs, which exhibit diamond channels of 1.3 nm diameter, great chemical stability, and CO2 adsorption capacity, have been evaluated as catalysts for the CO2 cycloaddition reaction with epoxides. Catalytic experiments reveal that the micropore environments of these MOFs have an outstanding impact on catalytic activity. Remarkably, NU-912(Hf)-I serves as an efficient heterogeneous catalyst for this catalytic reaction under mild conditions due to the high density of Lewis acid Hf6 cluster centers and strong Lewis base functional groups, surpassing most of the reported MOF-based catalysts.

One-Pot Synthesis of Styrene Derivatives from Allyl Silanes via B(C6F5)3-Catalyzed Isomerization-Hiyama Coupling.

Herein, we report a one-pot synthesis of styrene derivatives via a novel B(C6F5)3-catalyzed E-selective isomerization of readily accessible allyl silanes and subsequent Hiyama coupling of the versatile alkenyl silane intermediates. This one-pot, two-step approach enables access to a broad range of styrene derivatives, including those containing Lewis basic functional groups, that cannot be accessed via the previously developed B(C6F5)3-catalyzed isomerization of allyl benzenes.

Tailoring the Interfacial Interactions of Porous Polymer Membranes to Accelerate Atomic Layer Deposition: The Latent Path to Antifouling Membranes

Atomic layer deposition (ALD) is a powerful strategy to engineer hybrid organic-inorganic membranes with emergent functionalities. The combination of atomic-level thickness control, wide materials palette, and unprecedented conformality allow the physiochemical properties (e.g., hydrophilicity) of mesoporous polymer membranes to be precisely tuned. The nucleation of ALD materials growth on polymer surfaces relies on chemical interactions between the ALD metalorganic precursor and functional groups in the polymer structure and these interactions dictate the number of ALD cycles required to achieve a continuous coating. Strategies to enhance these interactions could enable desirable properties such as anti-fouling behavior to be imparted on inert polymer surfaces that lack the necessary functional groups for ALD nucleation. In this study, we demonstrate that the reactivity of polyacrylonitrile (PAN) membranes towards ALD metal oxide (MO) precursors with Lewis acid characteristics is enhanced by introducing Lewis base functional groups (amidoxime: Am) on the PAN backbone. The resulting Lewis acid-base interactions accelerates the MO nucleation in Am-PAN and reduce the number of deposition cycles required to achieve hydrophilicity compared to the untreated PAN membrane. Unveiling the reaction mechanism, the in-situ FTIR intensity changes established enhanced interaction dynamics between the ALD MO precursors and the Am-PAN membrane, unlike the PAN membrane. For similar MO cycles, through both spectroscopic and thermogravimetric analysis, we observe enhanced MO loading in the Am-PAN membrane compared to the PAN membrane. Here we have verified that strong Lewis acid-base interactions led to enhanced loading for a range of ALD MO materials including Al2O3, TiO2, SnO2, and ZnO. Most importantly, the Al2O3-Am-PAN hybrid membrane showed 23.3% higher antifouling capability compared to the pristine PAN membrane. Our approach expands the scope of design options for fouling-resistant porous hybrid inorganic-organic membranes and may reduce manufacturing costs of water treatment membranes.

Effective Dual-Functional Metal-Organic Framework (DF-MOF) as a Catalyst for the Solvent-Free Cycloaddition Reaction.

A new porous metal-organic framework, [Co (oba) (bpdh)]·(DMF) (TMU-63), containing accessible nitrogen-rich diazahexadiene groups was successfully prepared with the solvothermal assembly of 5-bis(4-pyridyl)-3,4-diaza-2,4-hexadiene (4-bpdh), 4,4'-oxybis(benzoic) acid (oba), and Co(II) ions. The combination of Lewis basic functional groups and porosity leads to high performance in CO2 adsorption and conversion in the cycloaddition reaction of epoxides under solvent-free conditions. To further enhance the catalytic efficiency of TMU-63, we introduced a highly acidic malonamide ligand into the structure via solvent-assisted ligand exchange (SALE) as a postsynthesis method. Incorporating different percentages of N1,N3-di(pyridine-4-yl) malonamide linker (4-dpm) into TMU-63 created a new porous structure. Powder X-ray diffraction (PXRD) and NMR spectroscopy confirmed that 4-bpdh was successfully replaced with 4-dpm in the daughter MOF, TMU-63S. The catalytic activity of both MOFs was confirmed by significant amounts of CO2 cycloaddition of epoxides under solvent-free conditions. The catalytic cycloaddition activities were found to be well-correlated with the Lewis base/Brønsted acid distributions of the materials examined in the TMU-63S series, showing that the concurrent presence of both acid and base sites was desirable for high catalytic activity. Furthermore, the heterogeneous catalysts could easily be separated out from the reaction mixtures and reused four times without loss of catalytic activity and with no structural deterioration.

Fine-tuning of pore-space-partitioned metal-organic frameworks for efficient C2H2/C2H4 and C2H2/CO2 separation

Acetylene (C2H2) and ethylene (C2H4) both are important chemical raw materials and energy fuel gasses. But the effective removement of trace C2H2 from C2H4 and the purification of C2H2 from carbon dioxide (CO2) are particularly challenging in the petrochemical industry. As a class of porous physical adsorbent, metal-organic frameworks (MOFs) have exhibited great success in separation and purification of light hydrocarbon gas. Herein, we rationally designed four novel MOFs by the strategy of pore space partition (PSP) via introducing triangular tri(pyridin-4-yl)-amine (TPA) into the 1D hexagonal channels of acs-type parent skeleton. By modulating the functional groups of linear dicarboxylate linkers for the parent skeleton, a series of isoreticular PSP-MOFs (SNNU-278−281) were successfully obtained. The synergistic effects of suitable pore size and Lewis basic functional groups make these MOFs ideal C2H2 adsorbents. The gas adsorption experimental results show that all MOFs have excellent C2H2 uptakes. Specially, SNNU-278 demonstrates a high C2H2 uptake of 149.7 cm3/g at 273 K and 1 atm. Meanwhile, SNNU-278−281 MOFs also show extremely great C2H2 separation from CO2 and C2H4. The optimized SNNU-281 with high-density hydroxy groups exhibits extraordinary C2H2/CO2 and C2H2/C2H4 dynamic breakthrough interval times up to 31 min/g and 17 min/g under 298 K and 1 bar.

Synthesis and Applications of Chiral Bicyclic Bisborane Catalysts

AbstractThe development of chiral borane Lewis acid catalysts opened the door for transition-metal-free catalyzed asymmetric organic reactions. Herein, we have summarized our work on the preparation of two classes of novel chiral bicyclic bisborane Lewis acid catalysts derived from C 2-symmetric [3.3.0] dienes and [4.4] dienes, respectively. These catalysts not only form frustrated Lewis pairs with Lewis bases to catalyze asymmetric hydrogenation reactions but also activate Lewis basic functional groups in traditional Lewis acid catalyzed asymmetric reactions.1 Introduction2 Synthesis of C 2-Symmetric Fused Bicyclic Bisborane Catalysts and Their Use in Imine Hydrogenation3 Synthesis of Spiro Bicyclic Bisborane Catalysts and Their Use in ­N-Heteroarene Reduction4 Other Types of Asymmetric Reactions Promoted by Chiral ­Bicyclic Bisborane Catalysts5 Conclusion

N‐Type Conjugated Polymer as Multi‐Functional Interfacial Layer for High‐Performance and Ultra‐Stable Self‐Powered Photodetectors Based on Perovskite Nanowires

AbstractHigh‐performance and long‐term stable self‐powered photodetectors (PDs) based on methylammonium lead iodide nanowires (NWs) are demonstrated by incorporating n‐type conjugated polymer poly{2,5‐bis(2‐dodecylhexadecyl)‐3,6‐di(thiophen‐2‐yl)pyrrolo‐[3,4‐c]pyrrole‐1,4(2H,5H)‐dione‐alt‐(E)‐1,2‐bis(3‐cyanothiophen‐2‐yl)ethene} (DPP‐CNTVT) as multi‐functional interfacial layer. Incorporating DPP‐CNTVT with abundant Lewis base functional groups can effectively passivate under‐coordinated Pb2+ defects, enabling perovskite NWs to exhibit remarkable stability and optoelectronic properties. Meanwhile, high electron mobility, together with the proper energy level of DPP‐CNTVT, makes it ideal for use as an electron transport layer. Particularly, by taking advantage of the low bandgap of DPP‐CNTVT, the utilization of low energy photons can be improved. The resulting PDs exhibit responsivity up to 0.50 A W−1, specific detectivity approaching 1014 Jones, and a wide linear dynamic range of nearly 265 dB under zero bias operation, which represent the best results ever reported for self‐powered perovskite PDs. More encouragingly, with the incorporation of an appropriate encapsulation layer, nearly 90% of the initial detectivity of PDs can be secured after 15 300 h of continuous operation in ambient conditions. The application of NWs PDs for solution‐processed reflective‐mode pulse oximetry is also demonstrated. This study provides valuable insights into developing efficient and ultra‐stable self‐powered perovskite PDs through interfacial engineering, which can accelerate the practical applications of this emerging technology.

Are rate and selectivity correlated in iridium-catalysed hydrogen isotope exchange reactions?

We have qualitatively examined the relationship between reaction rate and reaction selectivity in iridium-catalysed hydrogen isotope exchange (HIE) reactions directed by Lewis basic functional groups.

Directed Markovnikov hydroarylation and hydroalkenylation of alkenes under nickel catalysis.

We report a full account of our research on nickel-catalyzed Markovnikov-selective hydroarylation and hydroalkenylation of non-conjugated alkenes, which has yielded a toolkit of methods that proceed under mild conditions with alkenyl sulfonamide, ketone, and amide substrates. Regioselectivity is controlled through catalyst coordination to the native Lewis basic functional groups contained within these substrates. To maximize product yield, reaction conditions were fine-tuned for each substrate class, reflecting the different coordination properties of the directing functionality. Detailed kinetic and computational studies shed light on the mechanism of this family of transformations, pointing to transmetalation as the turnover-limiting step.

Launching Werner Complexes into the Modern Era of Catalytic Enantioselective Organic Synthesis.

Reactions catalyzed by transition metal complexes almost always entail binding of one or more reactants to the metal center, and nearly every corner of the "chiral pool" has been picked over in efforts to develop enantioselective catalysts. As reported by Alfred Werner in 1911-1912, salts of the formally D3-symmetric [Co(en)3]3+ trication (en = ethylenediamine) were among the first chiral inorganic compounds to be resolved into enantiomers. These air- and water-stable complexes are substitution-inert, so for 100 years they languished without application in organic synthesis. We then showed that when they are rendered soluble in organic media by lipophilic anions such as fluorinated tetraarylborates BArf-, they become potent catalysts for a variety of carbon-carbon and carbon-heteroatom bond forming reactions.These involve substrate activation by hydrogen bonding to the coordinated NH2 units (pKa ca. 15), a "second coordination sphere" mechanism. Only modest enantioselectivities are obtained with [Co(en)3]3+ 3BArf- or related chromium, rhodium, iridium, and platinum salts. However, high enantioselectivities are achieved when the three en ligands are replaced by the 1,2-diphenyl analogues (S,S)- or (R,R)-H2NCHPhCHPhNH2. Here only one BArf- anion is required to solubilize the trication, so a number of mixed-salt catalysts (2X-BArf-) have been evaluated. Alternatively, a dimethylamino group can be tethered to the backbone of one en ligand, providing bifunctional catalysts that obviate any need for an external base. Interestingly, the counteranions modulate the enantioselectivities somewhat. However, catalysts with chiral anions do not significantly outperform benchmark catalysts with achiral anions. Cagelike chiral hexaaminecobalt(III) complexes known as sepulchrates and sarcophagines, which feature secondary NH donor atoms, can also serve as catalysts, but the enantioselectivities are very low.In a spinoff application, certain salts are found to be superb "chiral solvating agents", leading to distinct sets of NMR signals for enantiomers of chiral analytes with Lewis basic functional groups. Loadings of 10-25 mol % generally suffice, providing the best way of assaying the enantiomeric purities of a host of compounds. Also, mixtures of several chiral compounds can be simultaneously analyzed. It is not surprising that complexes that perform well in chiral recognition phenomena also excel as enantioselective catalysts.In this Account, the stereochemical properties of the preceding complexes are treated, as well as arcana generally known only to specialists in the field. These include the use of charcoal for equilibrating configurations of the cobalt stereocenter and Sephadex for separating enantiomers and diastereomers. Other types of metal-containing hydrogen-bond-donor catalysts are briefly surveyed (noncoordinating NH units can also be effective), including several developed by other groups. However, the mechanisms of enantioselection in all of these transformations remain obscure. The optimum diastereomer and anion set varies from reaction to reaction, suggesting a "phenotypic plasticity" that allows adaption to a variety of processes.

Λ-[Co((S,S)-dpen)3]3+ 2I-B(C6F5)4-: A Second Generation Air- and Water-Stable Chiral Solvating Agent for Chirality Sensing (dpen = NH2CHPhCHPhNH2).

When CDCl3 solutions of chiral racemic molecules containing moderately Lewis basic functional groups are treated with the chiral solvating agent (CSA) Λ-[Co((S,S)-dpen)3]3+ 2I-B(C6F5)4- (Λ-(S,S)-13+ 2I-B(C6F5)4-), baseline-resolved NMR signals are observed for the enantiomers (29 diverse analytes). Only 0.62-100 mol % loadings are required (avg 14.5 or 11.6% for 24 analytes common to all tested CSAs). The overall performance is superior to those reported earlier for analogous salts with 2X-BArf- counter anion sets [BArf = B(3,5-C6H3(CF3)2)4]; 1.0-100 mol % loadings, avg 32.6% (X = Cl) or 14.0% (X = I) for 24 common analytes) and a new 2TfO-B(C6F5)4- salt (1.1-100 mol % loadings; avg 31.0% for 24 common analytes), including extensions to prochirality sensing. The effect of the solvent (Δδ in CDCl3 > CD2Cl2) is analyzed. The new CSAs are prepared in two steps from Λ-(S,S)-13+ 3Cl- by standard anion metathesis recipes (90-98% overall). The broad analyte scope and modest loading requirements for the title CSA distinctly surpass those of others in the literature.

Constructing Unique Cathode Interface by Manipulating Functional Groups of Electrolyte Additive for Graphite/LiNi0.6Co0.2Mn0.2O2 Cells at High Voltage

A novel electrolyte additive, 1-(2-cyanoethyl) pyrrole (CEP), has been investigated to improve the electrochemical performance of graphite/LiNi0.6Co0.2Mn0.2O2 cells cycling up to 4.5 V vs Li/Li+. The 4.5 V cycling results present that after 50 cycles, up to 4.5 V capacity retention of the graphite/LiNi0.6Co0.2Mn0.2O2 cell is improved significantly from 27.4 to 81.5% when adding 1% CEP to baseline electrolyte (1 M LiPF6 in EC/EMC 1:2, by weight). Ex situ characterization results support the mechanism of CEP for enhancing the electrochemical performance. On one hand, the significant enhancement is ascribed to a formed superior cathode interfacial film by preferential oxidation of CEP on the cathode electrode surface suppressing electrolyte decomposition at high voltage. On the other hand, the duo Lewis base functional groups can effectively capture dissociation product PF5 from LiPF6 with the presence of an unavoidable trace amount of water or aprotic impurities in the electrolyte. Thus this mitigates the hydrofluoric acid (HF) generation that leads to the reduction of transition-metal dissolution in the electrolyte upon cycling at high voltage. The theoretical modeling suggests that CEP has a mechanism of stabilizing electrolyte via combination of -C≡N: functional group and H2O. The work presented here also shows nuclear magnetic resonance spectra analysis to prove the capability of CEP reducing HF generation and X-ray photoelectron spectroscopy analysis to observe cathode surface composition.

The robust, readily available cobalt(iii) trication [Co(NH2CHPhCHPhNH2)3]3+ is a progenitor of broadly applicable chirality and prochirality sensing agents.

When NMR spectra of chiral racemic organic molecules containing a Lewis basic functional group are recorded in the presence of air and water stable salts of the cobalt(iii) trication [Co((S,S)-NH2CHPhCHPhNH2)3]3+ (23+), separate signals are usually observed for the enantiomers (28 diverse examples, >12 functional groups). Several chiral molecules can be simultaneously analyzed, and enantiotopic groups in prochiral molecules differentiated (16 examples). Particularly effective are the mixed bis(halide)/tetraarylborate salts Λ-23+ 2X-BArf- (X = Cl, I; BArf = B(3,5-C6H3(CF3)2)4), which are applied in CD2Cl2 or CDCl3 at 1-100 mol% (avg 34 and 14 mol%). Job plots establish 1 : 1 binding for Λ-23+ 2Cl-BArf- and 1-phenylethyl acetate (4) or 1-phenylethanol (10), and ca. 1 : 2 binding with DMSO (CD2Cl2). Selected binding constants are determined, which range from 7.60-2.73 M-1 for the enantiomers of 10 to 28.1-22.6 M-1 for the enantiomers of 4. The NH moieties of the C2 faces of the trication are believed to hydrogen bond to the Lewis basic functional groups, as seen in the crystal structure of a hexakis(DMSO) solvate of Λ-23+ 3I-. These salts rank with the most broadly applicable chirality sensing agents discovered to date.

Proximity-Induced Reactivity and Product Selectivity with a Rationally Designed Bifunctional Peptide Catalyst

Cooperative catalytic systems are making significant advances in modern organic synthesis due to the potential to combine multiple catalytic cycles or enable enzyme-like proximity effects. We report the rational design of a bifunctional helical peptide catalyst that displays an imidazolidinone catalyst in close proximity to a thiourea binding site and enables proximity-enhanced reactivity and selectivity. The helical structure of the peptide and the binding of both reactants are shown to be essential for enhanced reactivity in Diels–Alder and indole alkylation reactions, and up to 28 000 catalyst turnovers are achieved. A variety of Lewis basic functional groups facilitate binding and proximity-enhanced reactivity, and product selectivity is observed that cannot be achieved in the absence of the peptide template.

Dehydrogenative Transformations of Imines Using a Heterogeneous Photocatalyst.

Heterogeneous semiconductors are underexploited as photoredox catalysts in organic synthesis relative to their homogeneous, molecular counterparts. Here, we report the use of metal/TiO2 particles as catalysts for light-induced dehydrogenative imine transformations. The highly oxophilic nature of the TiO2 surface promotes the selective binding and dehydrogenation of alcohols in the presence of other oxidizable and Lewis basic functional groups. This feature enables the clean photogeneration of aldehyde equivalents that can be utilized in multicomponent couplings.