Coplanar Atropochiral 5H-Cyclopenta[2,1-b:3,4-b']dipyridine Ligands: Synthesis and Applications in Asymmetric Ring-Opening Reaction.

Bipyridines represent a class of ligands renowned for their versatility and efficacy in numerous transition metal-catalyzed reactions. Chiral bipyridine ligands are noted for their distinctive reactivity and stereoselectivity. In this work, we have designed and synthesized a class of bipyridine ligands endowed with an axially chiral scaffold. These ligands feature: (a) a precisely aligned coplanar bipyridine framework that is beneficial for metal chelation; (b) a spacious environment around the metal-bipyridine complexes, capable of hosting substrates with substantial steric bulk; (c) a chiral pocket induced by the axially chiral architecture. These atropochiral planar bipyridine ligands were successfully applied in copper-catalyzed ring-opening reactions of cyclic diaryliodoniums with bulky secondary amines, achieving high efficiency and stereoselectivity that were unsuccessful in our previous efforts.

Regio- and Atroposelective Ring-Opening of 1H-Benzo[4,5]oxazolopyridinones.

The development of new methods for regio- and stereoselective activation of C-O bonds in ethers holds significant promise for synthetic chemistry, offering advantages in terms of environmental sustainability and economic efficiency. Moreover, the C-N atropisomers represent a fascinating and crucial chiral system, extensively found in natural products, pharmaceutical leads, and the frameworks of advanced materials. In this work, we have introduced a nickel-catalyzed regio- and enantioselective carbon-oxygen arylation reaction for atroposelective synthesis of N-arylisoquinoline-1,3(2H,4H)-diones. The high regioselectivity of C-O cleavage benefits from the high stability of the in situ formed (amido)ethenolate via oxidative addition. Additionally, the self-activation of the aryl C-O bond facilitates the reaction under mild conditions, leading to outstanding enantioselectivities. The diverse post-functionalizations of the axially chiral isoquinoline-1,3(2H,4H)-diones further highlighted the utility of this protocol in preparing valuable C-N atropisomers, including the chiral phosphine ligands.

Atroposelective Three-Component Coupling of Cyclic Diaryliodoniums and Sodium Cyanate Enabled by the Dual-Role of Phenol.

A copper-catalyzed atroposelective ring-opening reaction of cyclic diaryliodoniums, sodium cyanate (NaOCN) and phenols is reported. The reaction chemoselectively affords axially chiral carbamates by sequential coupling of cyclic diaryliodonium and NaOCN, followed by phenol. Mechanistic investigations revealed that phenol is not only a reagent to trap highly active intermediate isocyanates, but it also activates the copper catalyst as a standby ligand. The carbamates were readily transformed into highly functionalized urea derivatives within a simple nucleophilic substitution reaction.

Diols Activation by Cu/Borinic Acids Synergistic Catalysis in Atroposelective Ring-Opening of Cyclic Diaryliodoniums.

A Cu-catalyzed enantioselective ring-opening alkoxygenation reaction of cyclic diaryliodonium salts and diols in the presence of borinic acids was reported. Tuning structure of borinic acids with six or five-membered ring skeleton could selectively activate 1,2-diols or 1,4-diols. A catalytic cycle through a key ion pair model that accounts for the observed enantioselectivity was proposed.

Luminol-Eu3+-Gd3+-functionalized mesoporous silica for ultrasensitive detection of tetracycline antibiotics and smartphone-assisted sensing analysis.

An organic-inorganic hybrid nanoprobe, namely LML-D-SBA@Eu3+-Gd3+, was constructed, with SBA-15 acting as the carrier material, and luminol and Eu3+ acting as fluorescence channels to achieve ratiometric signals that eliminate external interference (accurate detection). Gd3+ was used as a sensitizer to amplify the red emission of Eu3+ (ultrasensitive detection). In TCs detection, the luminol emission at 428 nm was quenched due to the photoinduced electron transfer mechanism, and the Eu3+ emission at 617 nm was sensitized due to the synergistic energy transfer from TCs and Gd3+ to Eu3+. The fluorescence intensity at 617 and 428 nm showed ratiometric changes as indicated by notable color changes from blue to red. The detection limits for TC and OTC were 0.21 and 0.08 ng/mL, respectively. To realize a facile, rapid, and cost-effective detection, we constructed a portable intelligent sensing platform based on smartphones, and it demonstrated great potential for on-site detection of TCs.

Kinetic Resolution of Helicenols via Palladium-Catalyzed Atroposelective C-C Bond Cleavage/Ring-Opening Reaction.

Helicenes represent a class of inherently chiral structures that lack conventional chiral elements, such as stereogenic centers, chiral axes, or plane. The asymmetric synthesis of these helical compounds can be particularly challenging as a result of their pronounced molecular strain. In this study, we report a palladium-catalyzed atroposelective carbon-carbon bond cleavage reaction of helical tertiary alcohols. Because the helical alcohols are configurationally stable, the reaction proceeded through a kinetic resolution pathway, resulting in achieving optically active helicenols alongside the sterically hindered axially chiral products.

Pivotal Role of Modifiable A-Site Doping in Enhancing Valence Stability and Excited State Dynamics of MnO6.

The controlled regulation of A-site in rare earth manganate perovskites can orderly arrange the electronic states, leading to the emergence of unique transport properties. However, it is challenging to balance crystal structure stability and property variations during the multi-ion doping. In this study, a series of multivalent manganate perovskites are synthesized by hydrothermal method through the A-site multielement doping, which enables the manganese atoms with varying valence states to orderly arrange at the B site. Powder X-ray diffraction (PXRD) and X-ray absorption spectra (XAS) confirm that the splitting of the K─O hybrid orbitals in the crystal effectively prevents any distortion of the MnO6 octahedron, thereby facilitating the ordered arrangement of Mn (III) -Mn (IV) -Mn (V) at the B-site and promoting superstructure formation. The transient absorption spectra (TAS) reveals that the sequential arrangement of Mn (III) - Mn (IV) - Mn(V) better forms the charge transfer channels, and thereby makes the photodynamic properties of the sample composition-dependent. These photodynamic properties will facilitate the study of exciton-electron coupling behavior in LCKMO crystals during electrical transport.

Conjugation-Induced Spin Delocalization in Helical Chiral Carbon Radicals via Through-Bond and Through-Space Effects.

A class of highly stable hydrocarbon radicals with helical chirality are synthesized, which can be isolated and purified by routine column chromatography on silica gel. These carbon-centered radicals are stabilized by through-bond delocalization and intramolecular through-space conjugation, which is evidenced by Density Functional Theory (DFT) calculation. The high stability enables to directly modify the carbon radical via palladium-catalyzed cross-coupling with the radical being untapped. The structures and optoelectronic properties are investigated with a variety of experimental methods, including Electron Paramagnetic Resonance (EPR), Ultraviolet Visisble Near Infrared (UV-vis-NIR) measurements, Cyclic Voltammetry (CV), Thermogravimetry Analysis (TGA), Circular Dichroism (CD) spectra, High-Performance Liquid Chromatography (HPLC), and X-ray crystallographic analysis. DFT calculations indicated that the 9-anthryl helical radical is more stable than its tail-to-tail σ-dimer over 13.2 kJ mol-1 , which is consistent with experimental observations.

Divergent Synthesis of Helical Ketone Enabled by Rearrangement of Spiro Carbocation.

An acid-mediated electrophilic cyclization of 2-alkynyl-1,1'-biphenyls for the divergent synthesis of angular, bent, and zigzag fused nonplanar conjugated organic molecules was realized. The key feature of this reaction is a Wagner-Meerwein-type rearrangement via a spiro carbocation intermediate, which was formed by electrophilic cyclization of the 9H-fluoren-9-one derivative at the meta position. The products can be advanced to helical fluorenes, which exhibit high fluorescence quantum yields.

Rhodamine derivative-functionalized mesoporous silica-Al3+ hybrid material for fluorescence "turn-on" detection of tetracycline antibiotics in aqueous media.

The organic-inorganic hybrid material was prepared by embedding 2-amino-3',6'-bis(diethylamino)spiro[isoindoline-1,9'-xanthen]-3-one (RBH) onto mesoporous SBA-15 silica and coordinating it with Al3+ (RBH-SBA-15-Al3+). RBH-SBA-15-Al3+ was used for the selective and sensitive detection of tetracycline antibiotics (TAs) in aqueous media based on the binding site-signaling unit mechanism, in which Al3+ acted as the binding site and the fluorescence intensity at 586 nm as the response signal. The addition of TAs to RBH-SBA-15-Al3+ suspensions resulted in the formation of RBH-SBA-15-Al3+-TAs conjugates, which realized the electron transfer process and turned-on fluorescence signal at 586 nm. The detection limits for tetracycline (TC), oxytetracycline, and chlortetracycline were 0.06, 0.06, and 0.03 µM, respectively. Meanwhile, the detection of TC was feasible in real samples, such as tap water and honey. In addition, RBH-SBA-15 can operate as a TRANSFER logic gate by using Al3+ and TAs as input signals and the fluorescence intensity at 586 nm as output signal. This study proposes an efficient strategy for the selective detection of target analytes by introducing interaction sites (e.g. Al3+) with target analytes in the system.

Enantioselective preparation of atropisomeric biaryl trifluoromethylsulfanes via ring-opening of cyclic diaryliodoniums.

Two convenient and practical methods for the synthesis of axially chiral biaryls bearing the trifluoromethylthio group are reported. A Cu-catalyzed enantioselective ring-opening reaction of cyclic diaryliodoniums with CsSCF3 enables the direct synthesis of trifluoromethylthiolated biaryl atropisomers in high yields and enantioselectivity. For unsymmetric cyclic diaryliodoniums bearing an adjacent group to the C-I bond, a two-step procedure is required to achieve good regio- and enantioselectivity.