A novel visible-light-driven organocatalytic protocol to access aerobic oxidative cleavage of olefins, promoted by sodium benzene sulfinate, is described herein. An array of alkenes smoothly delivered the corresponding aldehydes and ketones under transition-metal-free conditions. Notably, α-halo-substituted styrenes proceeded with photoinduced oxidation to finally afford α-halo-acetophenones with halogen migration. Crucial to this oxidation was the formation of charge-transfer complexes between sodium benzene sulfinate with molecular O2 to ultimately deliver the carbonyl products.

A manganese succinate having a layer structure in which the layers are pillared by the isonicotinate spacers in a 3D architecture exhibits long-range ferrimagnetic order below 5.0 K, with the ferrimagnetism arising, for topological reasons, from the nature of the carboxylate binding modes. The compound is the first structurally authenticated example of a 3D ferrimagnet, featuring a homometallic topological ferrimagnetic sheet among metal carboxylates.

The first structurally authenticated example of coordinated polymer featuring homometallic pillared-trilayer structure, [Co(3)(ina)(2)(pico)(2)(H(2)O)(2)](n) (1), was built from mixed pyridyl-type monocarboxylates, isonicotinate (ina) and 3-hydroxypicolinate (pico), containing Kagome-type [Co(3)(pico)(2)(H(2)O)(2)](n)(2n+) trilayers. The magnetic phase diagram of 1 shows a metamagnetic transition below 3.2 K, arising from the competing interactions between the antiferromagnetic intralayer couplings in different amplitudes with obviously noncompensated moments versus weak AF interlayer coupling.

A new pillared-layer coordination polymer, [Co(3)(pybz)(2)(pico)(2)](n) (1; pybz = 4-(pyridin-4-yl)benzoate, pico = 3-hydroxypicolinate), contains rare 2D [Co(3)(pico)(2)](n)(2n+) layers formed by linear cobalt(II) trimers through the unusual mu(4)-kappaN,O:kappaO'-mu(2):kappaO''-mu(2) bridging mode of pico ligands, which are further cross-pillared by exotridentate bridging pybz ligands to form a three-dimensional structure with an unusual uninodal 8-connected body-centered-cubic topology. The bulk magnetic behavior of 1 exhibits ferrimagnetic long-range ordering below 2.6 K, which mainly arises from the cooperative magnetic effect of the intra- and intertrimer arrangements in the 2D magnetic system based on the nature of the exchange modes of mu(2)-hydroxyl, mu(2)-carboxylate oxygen, and 1,1,3-mu(3)-carboxylate bridges.

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A visible-light-induced defluorinative dichloromethylation of α-CF3 alkenes was developed with cheap and readily accessible chloroform simultaneously as a dichloromethylation reagent and reaction medium, leading to the facile preparation of new polyhalogenated scaffolds. Notably, the change from CHCl3 to CDCl3 offers a straightforward pathway for accessing the deuterated analogues with excellent degrees of D incorporation. Mechanistic studies suggested the reaction underwent a radical addition of the dichloromethyl radical with alkenes, followed by sequential single-electron transfer and defluorination. This protocol features mild conditions, easy operation, facile scalability, and high efficiency, allowing convenient access to dichloronated gem-difluoroalkenes.

A new cycloartane-type triterpene glycoside, namely soulieoside M (1), and one known compound, beesioside I (2), were isolated from the ethanolic extract of the rhizomes of Souliea vaginata. Their structures were determined spectroscopically and compared with previously reported spectral data. Compounds 1 and 2 were evaluated for their cytotoxic activities against three human cancer cell lines.

Herein, readily available and inexpensive CDCl 3 was first identified as a new trideuteromethylation reagent under photoredoxcatalyzed conditions. Thus, a facile photocatalytic protocol for the C−H trideuteromethylation of quinoxalin-2(1H)-one was achieved. This operationally straightforward transformation displays a broad scope and provides a new route to introduce the trideuteromethyl group (CD 3 ) with excellent levels of deuterium content.