Total synthesis of the tetracyclic indole alkaloid ht-13-B.

An expedient synthesis corroborating the proposed structure of the tetracyclic indole alkaloid ht-13-B is presented. Key synthetic steps include acyliminium ion allylation, a Mitsunobu reaction, a palladium-catalyzed Stille-Kelly cross coupling reaction, and a carbon monoxide-mediated palladium-catalyzed reductive N-heterocyclization. The chiral centers are ultimately derived from commercially available trans-4-hydroxy-l-proline.

Spin-glass behavior of a hierarchically-organized, hybrid microporous material, based on an extended framework of octanuclear iron-oxo units.

Inspired by the stepwise addition of octanuclear iron units into mammalian ferritin, a "stop-and-go" synthesis strategy was used to prepare two microporous (Langmuir surface area, 490 m(2) g(-1); effective pore size, 4-5 Å) hierarchical materials {[Fe8(µ4-O)4(µ-pz)12Cl0.3(µ-O)1.85}n () and {[Fe8(µ4-O)4(µ-4-Me-pz)12Cl0.4(µ-O)1.8}n (), which are new members of the EO2 family of polymeric materials (E = C, Si and Ge). The secondary building units (SBUs) E = [Fe8(µ4-O)4(µ-4-R-pz)12] (Fe8) are nanoscale pseudo-spherical clusters, rather than single atoms, forming µ-oxo Fe-O-Fe linkages between Fe8-SBUs. The characteristic Fe-O-Fe asymmetric stretching mode in the infrared (IR) spectra of these compounds appearing at around 800 cm(-1) suggest the formation of approximately linear µ-oxo Fe-O-Fe linkages between Fe8-SBUs in and . We employ the concept of continuous random network (CRN) to describe for the first time the framework features of a Fe8-based amorphous materials, in which the average connecting numbers of each Fe8-cluster are ∼3.7 and ∼3.6 for and , respectively. (57)Fe-Mössbauer spectroscopic analysis provides insights to the intercluster connectivity of and on one hand and to their magnetic properties on the other, evident by a magnetic split sextet below 30 K. The combination of Mössbauer spectroscopy and magnetism measurements reveals a spin-glass behavior with Tg of ∼30 K. The hierarchical porous materials and straddle the gap between metal oxides and metal-organic frameworks (MOFs). This study may open an alternative way for the development of multifunctional materials based on high nuclearity metal clusters.

Curing of a bisphenol E based cyanate ester using magnetic nanoparticles as an internal heat source through induction heating.

We report on the control of cyclotrimerization forming a polycyanurate polymer using magnetic iron oxide nanoparticles in an alternating-current (ac) field as an internal heat source, starting from a commercially available monomer. Magnetic nanoparticles were dispersed in the monomer and catalytic system using sonication, and the mixture was subjected to an alternating magnetic field, causing the magnetic nanoparticles to dissipate the energy of the magnetic field in the form of heat. Internal heating of the particle/monomer/catalyst system was sufficient to start and sustain the polymerization reaction, producing a cyanate ester network with conversion that compared favorably to polymerization through heating in a conventional laboratory oven. The two heating methods gave similar differential scanning calorimetry temperature profiles, conversion rates, and glass transition temperatures when using the same temperature profile. The ability of magnetic nanoparticles in an ac field to drive the curing reaction should allow for other reactions forming high-temperature thermosetting polymers and for innovative ways to process such polymers.