The biochemistry of cell-adhesion

The proposition is examined that adhesion between cells of animal tissues, and between cells and their extracellular matrix, is brought about by specific molecules present at cell-surfaces. Evidence is surveyed which has begun to emerge from the use of antibodies which inhibit or reverse adhesion. Putative cell-adhesion molecules in cellular slime-moulds and cells of chick and mouse embryos have been identified by their ability to neutralize the adhesion-inhibiting activity of monovalent fragments of polyspecific antibodies. In some instances antibodies have also been used to investigate the role of the cell-adhesion molecules in morphogenetic phenomena. A possible parallel is discussed between the effects of calcium ions on the cell-adhesion molecule uvomorulin from mouse blastomeres, and its effects on certain other cell-adhesion molecules.Although the role of fibronectin in promoting attachment and spreading of cells on artificial substrates and on denatured collagen is firmly established, there is little evidence that this glycoprotein is involved in direct intercellular adhesion. The observation that cells spread on adsorbed fibronectin, whereas binding of individual fibronectin molecules to cells is difficult to demonstrate may merely indicate that fibronectin is a relatively weak ligand for cell-surfaces. It is suggested that rather than being a necessary intermediate in the adhesion of cells to collagen, fibronectin may form matrix in its own right which shares with native collagen the ability to promote cell-attachment and spreading.The long-held view that cell-surface oligosaccharides act as receptors in cell-adhesion appears still to be largely unsubstantiated. However the poorly adhesive properties of cells from many different lines with glycosylation defects strongly suggest N-linked oligosaccharides of glycoproteins are involved in some way as yet not determined.     

Study of isotope exchange reactions by double labelling

This paper presents the method of double labelling in the study of the kinetics of homogeneous isotope exchange reactions. This method was tested by the determination of the Sn(II)−Sn(IV) exchange rate in hydrochloric acid medium. The system was labelled by the tracer^119mSn [initially in the Sn(IV) state]; when the isotope equilibrium was established, Sn(IV) was again labelled by tracer¹¹³Sn. The separation of Sn(II) and Sn(IV) in the given time of exchange was performed by the extraction of Sn(IV)-hydroxyquinolate into chloroform. The specific activities of the separated components were determined from the ratio of¹¹³Sn and^119mSn activities. The exchange rate was calculated from the time dependence of specific activities. The advantage and possibilities of the method of double labelling in the study of isotope exchange are discussed.     

Frictional properties of dilute block-copolymer solutions and homopolymer solutions. Application to molecular weight determination.

An equation for the translational diffusion coefficient of block copolymers in dilute solution has been obtained by modifying Zimm's equation for homopolymers to take into account the existence of dissimilar segments in block copolymers. Illustrative calculations for homopolymers and block copolymers have been made and the results for homopolymers have been compared with experiments and with the calculations of Yamakawa and Fujii. A procedure has been proposed to determine the molecular weight of a block copolymer from measurements of its limiting viscosity number and its sedimentation coefficient or translational diffusion coefficient.     

The Raman active internal vibrational modes of potassium nitrate

The Raman active internal vibrational modes of single crystal orthorhombic potassium nitrate have been studied in various polarizations. The full multiplet structure predicted by factor group analysis for the v₂ and v₃ regions has been observed for the first time. The expected site group splitting of the v₄ mode was not observed and can be assumed to be less than 0.5 cm^?1.     

Fluorescence of Xe2 molecules in the vacuum-ultraviolet

Fluorescence of the Xe₂ continuum between 1460 and 1800 Å has been observed during excitation of Xe₂ molecules with CO fourth positive bands from a microwave discharge lamp. Fluorescence spectra at different Xe and added gas pressures show that in collisions with Xe or Kr atoms, the excited Xe₂ diatoms are efficiently relaxed to low vibrational levels of the ¹Σ_u⁺ and ³Σ_u⁺ potentials without being quenched noticeably. With Kr the rate constant for relaxation out of the primarily excited high vibrational levels is found to be about 3×10^?11 cm³ molecule^?1 s^?1.     

Metallkomplexe mit anionischen Liganden von Elementen der 4. Hauptgruppe. VIII. Pentacarbonyl-trihalogenstannido-metallat(O)-Komplexe von chrom,molybdän und wolfram mit fluor- und jodhaltigen stannidliganden

Metal Complexes with Anionic Ligands of Elements of the Main Group IV. VIII Pentacarbonyltrihalogenostannidometalate(O) Complexes of Chromium, Molybdenum, and Tungsten with Fluorine and Iodine Containing Trihalogenostannido Ligands In methylenechloride [As(C₆H₅)₄][SnF₃] readily reacts with the metalhexacarbonyls forming the arsoniumsalts of the pentacarbonyltrifluorostannidometalate(O) complexes, [M(CO)₅SnF₃]^? (M ? Cr, Mo, W). Exclusively by the reaction of the intermediately formed complex Cr(CO)₅THF only one pure triiodostannidometalate(O) Complex, [N(C₂H₅)₄][Cr(CO)₅SnJ₃], could be isolated. The trihalogenostannidometalate(O) complexes [M(CO)₅SnClX₂]^? (X ? F: M ? Cr, Mo, W; X ? J: M ? Cr) could be prepared by SnX₂-insertion reactions of the [M(CO)₅Cl]^? complexes. The bonding properties of the halogenostannide ions are discussed on the bases of the IR spectra of their metalate(O) complexes.     

NMR and stereochemical studies of non aromatic heterocyclic compounds—II : 13C and 31P NMR of 2-methoxy-1,3,2-dioxaphosphorinanes

¹³C and ³¹P chemical shift data for eight 2-methoxy-1,3,2-dioxaphosphorinanes are reported. Examination of pairs of geometrical isomers, which differ only in the orientation of the OMe substituent on P^III, have shown that both the ³¹P and the ¹³C signals of C_4,6 atoms appear 3–4 ppm at higher field when the OMe is axial compared with the equatorial isomer. This observation can be associated with the 1–3 syn diaxial interaction between the phosphorus axial substituent and the axial hydrogens on C_4,6 and should thus constitute, in the future, a supplementary tool for the structural analysis of this kind of compound. Important long range δ effects were observed both on ¹³C and especially on ³¹P chemical shifts. It is suggested that the high field δ_e effects could reflect a direct stereoelectronic interaction between the P atom and the cyclic C-5 atom. This interpretation is supported by a study of the ³¹P…¹³C coupling constants and their stereochemical dependence.     

Die Analytik wasserl?slicher Cellulose?ther

Zusammenfassung Es werden allgemeine und qualitative Merkmale von Natrium-Carboxymethylcellulose, Methylcellulose und Hydroxyäthylcellulose sowie gravimetrische und titrimetrische Bestimmungsmöglichkeiten der wasserlöslichen Celluloseäther insbesondere im Zusammenhang mit dem Substitutionsgrad beschrieben.Verfahren zur Ermittlung der Viscosität von Lösungen, des Polymerisationsgrades und des Gelteilchengehaltes werden besprochen. Abschließend werden charakteristische Beispiele für das analytische Vorgehen bei Substanzgemischen gegeben, die nur einen geringen Anteil Celluloseäther enthalten.

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Analysis of water-soluble cellulose ethers

General and qualitative characteristics of sodium carboxymethylcellulose, methylcellulose and hydroxyethylcellulose are presented and gravimetric and titrimetric methods for the determination of water-soluble cellulose ethers are described, especially with regard to the degree of substitution. Procedures for the measurement of the viscosity of solutions, of the degree of polymerisation and of the content of gel particles are discussed. Characteristic examples are presented for the treatment of mixtures containing only a small percentage of cellulose ethers.

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Erweiterte und umgearbeitete Fassung eines Vortrages, gehalten am 28. 6. 1971 in Baden-Baden.

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Frau Dr. G. Bartelmus, Analyt. Laboratorium der Fa. Kalle AG, sprechen wir an dieser Stelle unseren herzlichen Dank für wertvolle Beratung aus.     

A mechanistically guided design leads to the synthesis of an efficient and practical new reagent for the highly enantioselective,catalytic dihydroxylation of olefins

[structure: see text] The catalytic asymmetric dihydroxylation of olefins has been accomplished with high enantioselectivities using a proline-based catalyst. The pre-transition-state assembly for styrene is shown.     

Teaching nuclear and radiochemistry at undergraduate colleges

A large fraction of the potential graduate students in chemistry come from undergraduate colleges. The exposure of these students to the field of nuclear and radiochemistry is limited by the fact that few professionals actively involved in the field teach at these schools. There is also increasing competition for the limited number of chemistry students by other chemical specializations. Innovative approaches such as a short course to introduce students to nuclear and radiochemistry and some of the needs for undergraduate teaching are discussed.