다중혈관 관상동맥 환자에서 y-문합을 이용하여 양쪽 내흉동맥만을 사용한 우회술의 조기 성적

I read this book the same weekend that the Packers took on the Rams, and the experience of the latter event, obviously, colored my judgment. Although I abhor anything that smacks of being a handbook (like, \"How to Earn a Merit Badge in Neurosurgery\") because too many volumes in biomedical science already evince a boyscout-like approach, I must confess that parts of this volume are fast, scholarly, and significant, with certain reservations. I like parts of this well-illustrated book because Dr. Sj6strand, without so stating, develops certain subjects on technique in relation to the acquisition of judgment and sophistication. And this is important! So, given that the author (like all of us) is somewhat deficient in some areas, and biased in others, the book is still valuable if the uninitiated reader swallows it in a general fashion, realizing full well that what will be required from the reader is a modulation to fit his vision, propreception, adaptation and response, and the kind of problem he is undertaking. A major deficiency of this book is revealed by comparison of its use of physics and of chemistry to provide understanding and background for the application of high resolution electron microscopy to problems in biology. Since the volume is keyed to high resolution electron microscopy, which is a sophisticated form of structural analysis, but really morphology in a modern guise, the physical and mechanical background of The instrument and its ancillary tools are simply and well presented. The potential use of chemical or cytochemical information as it relates to biological fine structure , however, is quite deficient. I wonder when even sophisticated morphol-ogists will consider fixation a reaction and not a technique; only then will the fundamentals become self-evident and predictable and this sine qua flon will become less mystical. Staining reactions (the most inadequate chapter) ought to be something more than a technique to selectively enhance contrast of morphological elements; it ought to give the structural addresses of some of the chemical residents of cell components. Is it pertinent that auto-radiography gets singled out for more complete coverage than other significant aspects of cytochemistry by a high resolution microscopist, when it has a built-in minimal error of 1,000 A in standard practice? I don't mean to blind-side (in strict football terminology) Dr. Sj6strand's efforts for what is \"routinely used in our laboratory\"; what is done is usually well done. It's just that …

Methods in Enzymology.

: The unpolarized absorption and circular dichroism spectra of the fundamental vibrational transitions of the chiral molecule, 4-methyl-2-oxetanone, are calculated ab initio. Harmonic force fields are obtained using Density Functional Theory (DFT), MP2, and SCF methodologies and a 5S4P2D/3S2P (TZ2P) basis set. DFT calculations use the Local Spin Density Approximation (LSDA), BLYP, and Becke3LYP (B3LYP) density functionals. Mid-IR spectra predicted using LSDA, BLYP, and B3LYP force fields are of significantly different quality, the B3LYP force field yielding spectra in clearly superior, and overall excellent, agreement with experiment. The MP2 force field yields spectra in slightly worse agreement with experiment than the B3LYP force field. The SCF force field yields spectra in poor agreement with experiment.The basis set dependence of B3LYP force fields is also explored: the 6-31G* and TZ2P basis sets give very similar results while the 3-21G basis set yields spectra in substantially worse agreements with experiment. jg

Ab initio calculation of vibrational absorption and circular dichroism spectra using density functional force fields

Transition-metal (Fe, Co, Ni) based metal-organic framework materials with controllable structures, large surface areas and adjustable pore sizes have attracted wide research interest for use in next-generation electrochemical energy-storage devices. This review introduces the synthesis of transition-metal (Fe, Co, Ni) based metal-organic frameworks and their derivatives with the focus on their application in supercapacitors and batteries.

Transition‐Metal (Fe, Co, Ni) Based Metal‐Organic Frameworks for Electrochemical Energy Storage

More than a quarter of a century after the first metal template synthesis of a [2]catenane in Strasbourg, there now exists a plethora of strategies available for the construction of mechanically bonded and entwined molecular level structures. Catenanes, rotaxanes, knots and Borromean rings have all been successfully accessed by methods in which metal ions play a pivotal role. Originally metal ions were used solely for their coordination chemistry; acting either to gather and position the building blocks such that subsequent reactions generated the interlocked products or by being an integral part of the rings or "stoppers" of the interlocked assembly. Recently the role of the metal has evolved to encompass catalysis: the metal ions not only organize the building blocks in an entwined or threaded arrangement but also actively promote the reaction that covalently captures the interlocked structure. This Review outlines the diverse strategies that currently exist for forming mechanically bonded molecular structures with metal ions and details the tactics that the chemist can utilize for creating cross-over points, maximizing the yield of interlocked over non-interlocked products, and the reactions-of-choice for the covalent capture of threaded and entwined intermediates.

Strategies and tactics for the metal-directed synthesis of rotaxanes, knots, catenanes, and higher order links.

Bis-acyl-/aroyl-hydrazones as multidentate ligands

Extension of previous work on the lanthanide(III) ion complexes of p-tert-butyltetrathiacalix[4]arene has led to a variety of structurally characterised species containing oxo-, hydroxo- and aqua-ligands presumably derived from water present in the preparative medium, along with the thiacalixarene in various stages of deprotonation. The overall stoichiometry of some species is remarkably complicated due to the presence of simple anions and multiple solvents. Simplest is the binuclear complex [(μ-H2O){Ln(O-dmf)2}2(HL·dmf)2]·nS (dmf = dimethylformamide) [1Ln, Ln = Sm (nS = 2dmf), Eu (nS = 1.5dmf·2MeCN)], also the best-defined of all the arrays studied. The heaviest lanthanides give trinuclear Ln(OH)3·2Ln(LH)·xdmf·yH2O (2Ln, Ln = Yb, Lu), while both oxo and hydroxo species are isolable with Eu: trinuclear Eu3O(L)(LH)(LH4)·13dmf (3) and tetranuclear Eu4O(OH)2(L)(LH2)2(LH4)·12dmf (9), both somewhat atypical species containing uncoordinated thiacalixarene molecules within the lattice. Anion (NO3, ClO4) coordination, as in the tri- and tetranuclear species, 4–6Ln, 9, 10Ln, 11Ln, 12, seems especially favoured for the lighter lanthanides. In these arrays, the Ln3 and Ln4 aggregates are triangular or (quasi-)square-planar, except for Gd4O2(LH2)4·2H2O·2MeOH·2dmf·3.375CH2Cl2 (12), where there is a Z-disposition. Most common is an Ln3O core, which spans the gamut of Ln in three sets of crystal forms with cells of similar dimensions: for Ln = La...Nd, Ln3(OH)(NO3)4(LH2)2·4.5dmf (5Ln) (space group C2/m), and Sm...Lu, Ln3O(NO3)(LH)2·4H2O·2dmso·2MeCN·3py (6Ln) (space group P21/n), conformity with crystallographic symmetryentails disorder of the Ln atoms; in a further form of lowersymmetry Pn, (pyH)Ln3O(NO3)2(LH)2·2MeCN·xH2O·ydmso·1.5py·MeOH (7Ln, Ln = La, Ce), with no imposed crystallographic symmetry, some disorder persists, but none is found in the crystallographically unrelated form of 8Pr, Pr3O(NO3)(LH)2·16H2O·2MeCN·5py. Ln4(OH)(NO3)3(L)2·8dmf·2dmso·3H2O (10Ln, Ln = Pr...Gd, previously defined for Nd) has a square-planar Ln4O array sandwiched between a pair of L ligands, with a similar form found for Ln4O(ClO4)2(L2)·xdmf·yH2O (11Ln, Ln = La...Nd).

Systematic Structural Coordination Chemistry of p-tert-Butyltetrathiacalix[4]arene: Further Complexes of Transition-Metal Ions†

An overview is given of recent structural studies on heterometallic uranyl-containing species, with particular emphasis on those formed with carboxylate ligands, showing the effect of the additional metal cations and ancillary ligands on the dimensionality, geometry and topology of the assemblies generated. These examples illustrate the level of elaboration which is now possible in the design and synthesis of both uranyl clusters and coordination polymers, properties and potential applications of which are also briefly discussed.

Recent advances in structural studies of heterometallic uranyl-containing coordination polymers and polynuclear closed species

In discovering the remarkable catalytic properties of BINOL-derived phosphoramidites (binoP–NR2), Dutch researchers recently achieved a long-awaited breakthrough in asymmetric catalysis. For the first time, easily accessible monodentate chiral P(III) ligands turned out to provide high enantioselectivities when used in rhodium-catalysed olefin hydrogenation. The simplest ligand representative of this family is MonoPhos™, which can be made straightforwardly from BINOL and hexamethylphosphorous triamide. Since the first publication dealing with such catalysts (J. Am. Chem. Soc., 2000), a variety of binoP–NRR′ ligands have been reported in which the amino group bears a functional substituent or a stereogenic centre. This critical review examines the impact of the presence of such a functionality in the amino group on catalytic olefin hydrogenation reactions.

Jack Harrowfield

Papers

Bis-acyl-/aroyl-hydrazones as multidentate ligands

Systematic Structural Coordination Chemistry of p-tert-Butyltetrathiacalix[4]arene: Further Complexes of Transition-Metal Ions†

Recent advances in structural studies of heterometallic uranyl-containing coordination polymers and polynuclear closed species

BINOL-derived phosphoramidites in asymmetric hydrogenation: can the presence of a functionality in the amino group influence the catalytic outcome?

Analysis of trigonal-prismatic and octahedral preferences in hexaamine cage complexes