Heterogeneous Catalytic Oxidations with In Situ-Generated Hypervalent Iodine-Based Porous Organic Polymers.

Porous organic polymers (POPs) are novel emergent materials for heterogeneous organocatalysis owing to their remarkable physicochemical stabilities. Through a bottom-up approach entailing diligent design of twisted biaryl building blocks with in-built o-iodobenzoic acid (IA) moieties, a series of POP precatalysts, p-OMeIA-POP, DiMeIA-POP, and m-OMeIA-POP, were synthesized by employing Friedel-Crafts alkylation. These IA-POP precatalysts can undergo in situ oxidation in the presence of Oxone® to generate hypervalent iodine(V) species (λ5-iodanes), in particular, modified o-iodoxybenzoic acid, popularly termed IBX, which mediates diverse oxidative transformations.

A Comparative Analysis of Follicular Diameter Assessment Versus Doppler Ultrasound in Predicting Ovulation Timing for the Infertility Treatment: Insights From a Prospective Study.

Background Infertility remains a significant challenge affecting millions of couples worldwide, with ovulation abnormalities being a common underlying cause. Pharmacological methods, such as clomiphene citrate, are often used to stimulate ovulation. However, the optimal timing for sexual intercourse during ovulation induction remains contentious.

Synthesis of Acridone-Based Zn-Metal-Organic Framework (Zn-MOF) as a Photocatalyst: Application for Visible Light-Mediated Oxidation of Sulfides and Enaminones.

Acridone, a cyclic analogue of benzophenone that undergoes efficient intersystem crossing (ISC) to the triplet-excited state with near-unity quantum yield, was elaborated as a 3-connecting triacid linker, i.e., , to develop a photocatalytic metal-organic framework (MOF) for energy transfer applications; the triacid linker inherently features concave shapes, an attribute that is important for the construction of MOFs with significant porosity.

Synthesis and Excited-State Properties of Donor-Acceptor Azahelical Coumarins.

A set of three azahelical coumarins (s), namely, , , and , were rationally designed and synthesized, and their excited-state properties were comprehensively investigated. All three s are shown to display very high fluorosolvatochromic shifts as a result of significant intramolecular charge transfer in their excited states. The -quinoidal forms of the latter apparently contribute predominantly to large dipole moments in their excited states.

Visible Light-Induced Decomposition of Acyl Peroxides Using Isocyanides: Synthesis of Heteroarenes by Radical Cascade Cyclization.

Visible light-mediated facile synthesis of heteroarenes, namely, isoquinolines, benzothiazoles, and quinazolines, is demonstrated by employing isocyanides and inexpensive acyl peroxides. It is shown for the first time that singlet-excited isocyanides decompose acyl peroxides into aryl/alkyl radicals. The latter attack isocyanides, yielding imidoyl radicals that subsequently cyclize to afford heteroarene products.