Biomedical subjects
Publications and source records attributed to Jennifer A Moore.
The first examples of N,C-bonded beta-diketiminato phosphenium cations have been isolated as their triflate or tetrachloroaluminate salts, both of which have been structurally characterized.
The new Ar-BIAN complexes [(mes-BIAN)InCl(3)(THF)] (1), [(mes-BIAN)(2)Tl][PF(6)] (2), [(dipp-BIAN)SnCl(4)] (3), [(dipp-BIAN)SbCl(3)] (4), [(dipp-BIAN)BiCl(3)] (5) and [(mes-BIAN)BiCl(3)] (6) have been prepared by treatment of the neutral mes- and dipp-substituted BIAN ligands with the p-block reagents InCl(3), TlPF(6), SnCl(4), SbCl(3), and BiCl(3). The molecular structures of complexes 1-6 have been determined by single-crystal X-ray diffraction methods. However, only the atom connectivity was established for 5.
The Alkyl-BIAN ligands tert-Butyl-BIAN and 1-Adamantyl-BIAN have been synthesized and their structures have been determined by single-crystal X-ray diffraction along with that of the ZnCl2 complex of tert-Butyl-BIAN.
The first example of a phosphenium cation supported by N,N'-chelation of a beta-diketiminate ligand has been prepared and structurally characterized.
A 1 : 1 Lewis acid-base complex between CyN=C=NCy and PhBCl2 has been isolated and structurally characterized, heating of which in refluxing toluene results in the amidinate, [PhC{NCy}2]BCl2; the overall reaction has been modeled by DFT calculations.
The triple-decker cations trans-[(Cp*Sn)(2)(mu-eta(5):eta(5)-Cp*)](+) and trans-[(Cp*Pb)(2)(mu-eta(5):eta(5)-Cp*)](+) have been prepared and structurally characterized as their [B(C(6)F(5))(4)](-) salts from the reactions of [Cp*M][B(C(6)F(5))(4)](M = Sn, Pb) with the appropriate decamethylmetallocene. Both triple-decker cations adopt a cisoid arrangement of terminal Cp* groups, whereas the two known triple-decker main-group anions possess a transoid arrangement of terminal Cp groups. The reason for this conformational difference has been probed on the basis of DFT calculations.
The first example of a stable oxoborane monomer (LB=O) stabilized by complexation to AlCl3 has been prepared by the reaction of LAlCl2 with BCl3 followed by treatment with H2O in CH2Cl2 (L = [HC(CMe)2(NC6F5)2]). DFT calculations reveal that considerable boron-oxygen double bond character is retained in this complex.
Forest, agricultural, rangeland, wetland, and urban landscapes have different rates of carbon sequestration and total carbon sequestration potential under alternative management options. Changes in the proportion and spatial distribution of land use could enhance or degrade that area's ability to sequester carbon in terrestrial ecosystems. As the ecosystems within a landscape change due to natural or anthropogenic processes, they may go from being a carbon sink to a carbon source or vice versa. Satellite image analysis has been tested for timely and accurate measurement of spatially explicit land use change and is well suited for use in inventory and monitoring of terrestrial carbon. The coupling of Landsat Thematic Mapper (TM) data with a physiologically based forest productivity model (PnET-II) and historic climatic data provides an opportunity to enhance field plot-based forest inventory and monitoring methodologies. We use periodic forest inventory data from the U.S. Department of Agriculture (USDA) Forest Service's Forest Inventory and Analysis (FIA) Program to obtain estimates of forest area and type and to generate estimates of carbon storage for evergreen, deciduous, and mixed-forest classes. The area information is used in an accuracy assessment of remotely sensed forest cover at the regional scale. The map display of modeled net primary production (NPP) shows a range of forest carbon storage potentials and their spatial relationship to other landscape features across the southern United States. This methodology addresses the potential for measuring and projecting forest carbon sequestration in the terrestrial biosphere of the southern United States.