ABSTRACT
Neuropsychologists are increasingly being asked to apply neuropsychological test results to real world functioning; however, neuropsychological tests are not usually constructed to do so, but instead are more concerned with diagnostic accuracy than with prediction of daily functioning. Using samples of 5,460 patients that did self-ratings and 2791 patients that had family ratings plus the Meyers Neuropsychological Battery (MNB), it was found that the family ratings were better predicted by neuropsychological test data than were self-ratings on the 38 item Patient Competency Rating Scale (PCRS). The R values for family ratings on the 36 regression equations ranged from .236 to .763. The results show that the ratings given patients by family members could be predicted by the neuropsychological test results. These findings can help the clinician to make broad statements regarding likely real-life functioning and also support the ecological validity of the tests that make up the MNB.
ABSTRACT
Isocyanoazulenes (CNAz) constitute a relatively new class of isocyanoarenes that offers rich structural and electronic diversification of the organic isocyanide ligand platform. This article considers a series of 2-isocyano-1,3-X2-azulene ligands (X = H, Me, CO2Et, Br, and CN) and the corresponding zero-valent complexes thereof, [(OC)5Cr(2-isocyano-1,3-X2-azulene)]. Air- and thermally stable, X-ray structurally characterized 2-isocyano-1,3-dimethylazulene may be viewed as a non-benzenoid aromatic congener of 2,6-dimethyphenyl isocyanide (2,6-xylyl isocyanide), a longtime "workhorse" aryl isocyanide ligand in coordination chemistry. Single crystal X-ray crystallographic {Cr-CNAz bond distances}, cyclic voltametric {E1/2(Cr0/1+)}, 13C NMR {δ(13CN), δ(13CO)}, UV-vis {dπ(Cr) â pπ*(CNAz) Metal-to-Ligand Charge Transfer}, and FTIR {νN≡C, νC≡O, kC≡O} analyses of the [(OC)5Cr(2-isocyano-1,3-X2-azulene)] complexes provided a multifaceted, quantitative assessment of the π-acceptor/σ-donor characteristics of the above five 2-isocyanoazulenes. In particular, the following inverse linear relationships were documented: δ(13COtrans) vs. δ(13CN), δ(13COcis) vs. δ(13CN), and δ(13COtrans) vs. kC≡O,trans force constant. Remarkably, the net electron withdrawing capability of the 2-isocyano-1,3-dicyanoazulene ligand rivals those of perfluorinated isocyanides CNC6F5 and CNC2F3.
Subject(s)
Cyanides/chemistry , Electrons , Heterocyclic Compounds/chemistry , Isothiocyanates/chemistry , Azulenes/chemistry , Crystallography, X-Ray , Ligands , Magnetic Resonance Spectroscopy , Metals/chemistry , Models, Molecular , Molecular StructureABSTRACT
Reported are the synthesis and the crystal structures of the new ternary phases Sr3Cd8Ge4 and Eu3Cd8Ge4. The structures of both compounds have been established by single-crystal and powder X-ray diffraction methods. They crystallize in the tetragonal space group I4/mmm (No. 139, own structure type, Pearson symbol tI30) with Z = 2, and lattice parameters as follows: a = 4.4941(14) Å; c = 35.577(7) Å for Sr3Cd8Ge4, and a = 4.4643(12) Å; c = 35.537(9) Å for Eu3Cd8Ge4, respectively. The most prominent feature of the structure is the complex [Cd2Ge] polyanionic framework, derived by unique ordering of the Cd and Ge atoms in fragments that bear resemblance to the BaAl4 structure type. Temperature dependent DC magnetization measurements indicate that Eu3Cd8Ge4 displays Curie-Weiss paramagnetic behavior with no sign of magnetic ordering in the measured range. Theoretical considerations of the electronic structure on the basis of the tight-binding linear muffin-tin orbital (TB-LMTO-ASA) method are also presented and discussed.
ABSTRACT
Three synthetic routes to the unusual supramolecular complex ([Cp(2)Co](2)[{(OC)(5)V}(2)(µ-1,4-CNC(6)Me(4)NC)])(∞), which was crystallographically characterized, are presented. The dianion [{(OC)(5)V}(2)(µ-1,4-CNC(6)Me(4)NC)](2-) constitutes the first subvalent organometallics featuring a diisocyanoarene linker.
