Synthesis of some heterocyclic systems from nucleophilic substitution reactions with η6-o-dichlorobenzene-η5-cyclopentadienyliron hexafluorophosphate

A method for the synthesis of heterocylic systems related to 9,10-dihydroanthracene with two hetero-atoms at the 9,10-positions is described. It involves the nucleophilic substitution reaction of η⁶-o-dichlorobenzene-η⁵-cyclopentadienyliron hexafluorophosphate with two nucleophilic groups (OH, SH and/or NH₂) located in the 1,2-positions of a benzene ring to give a cyclopentadienyliron complexed heterocycle. Upon pyrolytic sublimation of the complex, the free heterocyclic compound is then obtained.     

Transformation of aminoacyl tRNAs for the in vitro selection of "drug-like" molecules

Evolutionary approaches are regularly used to isolate single molecules with desired activities from large populations of nucleic acids (approximately 10(15)). Several methods have also been developed to generate libraries of mRNA-encoded peptides and proteins for the in vitro selection of functional polypeptides. In principal, such mRNA encoding systems could be used with libraries of nonbiological polymers if the ribosome can be directed to polymerize tRNAs carrying unnatural amino acids. The fundamental problem is that current chemical aminoacylation systems cannot easily produce sufficient amounts of the numerous misacylated tRNAs required to synthesize a complex library of encoded polymers. Here, we show that bulk-aminoacylated tRNA can be transformed into N-monomethylated aminoacyl tRNA and translated. Because poly-N-methyl peptide backbones are refractory to proteases and are membrane permeable, our method provides an uncomplicated means of evolving novel drug candidates.     

Synthesis of some heterocyclic skeletons via organoiron complexes. Crystal and molecular structure of (5a,6,7,8,9,9a-η6-1,4-benzoxathiino[3,2-b]pyridine)(η5-cyclopentadienyl)iron hexafluorophosphate

Synthesis of the heterocyclic skeletons of some biologically active compounds from (η⁶-o-dichlorobenzene)(η⁵-cyclopentadienyrl)iron hexafluorophosphate in a two step procedure is described. Cyclopentadienyliron hexafluorophosphate complexes of 1,4-benzodioxino[2,3-b]pyridine, 1,4-benzoxathiino[3,2-b]pyridine, 10H-pyrido[3,2-b]benzoxazine, benzo[b]naphtho[2,3-e][1,4]dioxin, 4-methylbenzo[b]benzopyran-2-one[7,6-e][1,4]dioxin and benzo[b]anthracen-9,10-diono[1,2-e][1,4]dioxin were isolated and characterized. Upon pyrolytic sublimation of these complexes the free heterocycles were obtained and characterized. (η⁶-1,4-Benzoxathiino[3,2-b]pyridine)(η⁵-cyclopentadienyl)iron hexafluorophosphate crystalizes in the orthothombic system, space group Pbca; the dihedral angle between the planes of outer rings was found to be 176.8 (1).     

Following the cat: A preface for the next three papers

The three papers to follow, by Chris Rasmussen and three of his students, build from a task design the authors of this note developed in the 1990s. To introduce these papers, which extend our prior work in new directions, we sketch some background here.     

Connecting mem-models with classical theories

A family of mem-models, including the mem-dashpots, mem-springs, and most recently, mem-inerters, is emerging as a new and powerful way of capturing complex nonlinear behaviors of materials and systems under various types of dynamic loads involving different frequency, amplitude, and loading histories (e.g., hysteresis). Under the framework of nonlinear state-space representation and hybrid dynamical systems, mem-springs may be formulated to effectively represent an inherent degradation of material state. It is shown in this study, for the first time, how the absement (time integral of strain/displacement), a signature state variable for a mem-spring, can be connected with the damage variable, a key quantity in continuum damage mechanics. The generalized momentum (time integral of stress), on the other hand, is shown to be efficient in modeling strain ratcheting via the concept of mem-dashpot. It is also shown in this study, for the first time, how two formulations of the memcapacitive system models (for mem-springs) are special cases of the Preisach model.

     

Shape Matters: A Gold Nanoparticle Enabled Shape Memory Polymer Triggered by Laser Irradiation

With incorporation of gold nanoparticles, i.e., nanorods (AuNR) and nanospheres (AuNS), into a polyurethane‐based shape‐memory polymer (SMP) EG‐72D matrix, SMP nanocomposite films capable of being remotely triggered by low‐power laser are fabricated and characterized using UV‐vis‐NIR spectroscopy, X‐ray scattering, and dynamic mechanical analysis (DMA). It is demonstrated that, with incorporation of very low concentration of gold nanorods (≈0.1 wt%), the mechanically programmed EG‐72D/AuNR nanocomposite presents rapid response to low power laser irradiation (785 nm, ≈10 mW). Comparative studies on the laser irradiation response of EG‐72D/AuNS and EG‐72D/AuNR nanocomposite films suggest that AuNRs have significantly higher photothermal conversion efficiency than AuNS and on‐resonance laser irradiation, matching the wavelength of the incident laser with the longitudinal plasmon resonance of AuNR, is necessary to induce the fast response of gold nanoparticle enabled SMP nanocomposites.     

Imaging mitochondria in living corneal endothelial cells using autofluorescence microscopy

We report noninvasive autofluorescence mitochondrial imaging in cultured human corneal endothelial cells (HCECs). HCECs harvested from eye bank corneas were cultured in thin glass-bottom plates. Mitochondria were imaged with an autofluorescence microscope using a DAPI filter set (excitation: G365, emission: band pass 445/50) and then, after fixation with 4% paraformaldehyde, cells were stained with MitoTracker Green FM (MTG). Both images were aligned using a linear conformal algorithm for image mapping based on manually selected corresponding feature points, and then mathematically compared using two-dimensional spatial image correlation coefficients. Autofluorescence imaging provided highly resolved mitochondrial signals from living HCECs, comparable to those taken with MTG. Both techniques yielded very similar images at high magnification and high resolution, demonstrating the tubular morphology and cytoplasmic distribution that are characteristic of mitochondria. Image registration using a linear conformal mapping technique and cross-correlations showed high correlation of overlapping autofluorescence and MTG images. This study validates the novel use of autofluorescence vital imaging as a noninvasive, inexpensive and functional alternative to the mitochondria-specific dyes in cultured HCEC. This noninvasive mitochondrial imaging technique can be useful in future applications studying mitochondrial biology of ocular cells.