Supramolecular design of one-dimensional coordination polymers based on silver(I) complexes of aromatic nitrogen-donor ligands

VOLUME I Introduction The Incentive Physical-Chemical Properties Experimental Methods Quantitative Structure-Property Relationships (QSPRs) Mass Balance Models of Chemical Fate Data Sources and Presentation Illustrative QSPR Plots and Fate Calculations References Aliphatic and Cyclic Hydrocarbons Lists of Chemicals and Data Compilations Summary Tables and QSPR plots References Mononuclear Aromatic Hydrocarbons Lists of Chemicals and Data Compilations Summary Tables and QSPR plots References Polynuclear Aromatic Hydrocarbons (PAHs) and Related Aromatic Hydrocarbons Lists of Chemicals and Data Compilations Summary Tables and QSPR plots References VOLUME II * Halogenated Aliphatic Hydrocarbons Chlorobenzenes and Other Halogenated Mononuclear Aromatics Polychlorinated Biphenyls (PCBs) Chlorinated Dibenzop-dioxins Chlorinated Dibenzofurans VOLUME III * Ethers Alcohols Aldehydes and Ketones Carboxylic Acids Phenolic Compounds Esters VOLUME IV Nitrogen and Sulfur Compounds Lists of Chemicals and Data Compilations Summary Tables References Herbicides Lists of Chemicals and Data Compilations Summary Tables References Insecticides Lists of Chemicals and Data Compilations Summary Tables References Fungicides Lists of Chemicals and Data Compilations Summary Tables References APPENDICES List of Symbols and Abbreviations Alphabetical Index CAS Registry Index Molecular Formula Index * Each chapter contains lists of chemicals and data compilations, summary tables, QSPR plots, and references

Handbook of Physical-Chemical Properties and Environmental Fate for Organic Chemicals

Separations of lipids by silver ion chromatography.

A review of the nature and properties of chemicals present in pulp mill effluents

The dynamic coupled column liquid chromatographic (DCCLC) method for determining the solubility of polycyclic aromatic hydrocarbons (PAH) in water is described. The DCCLC technique is a very rapid, precise, and accurate method for determining the aqueous solubility behavior of sparingly soluble organic compounds. The agreement of PAH aqueous solubilities and calculated solubility parameters, such as ..delta..Hs, with values that have been previously reported in the literature helps to confirm the validity of this approach. In all cases replicate solubility measurements of the generated PAH solutions at constant temperature were better than +- 3 percent and in most cases better than +- 1%. The lack of an appropriate physical parameter for accurately extrapolating PAH solubilities further enhances the utility of DCCLC method.

R. M. Keefer

Papers

Cation Complexes of Compounds Containing Carbon--Carbon Double Bonds. IV. The Argentation of Aromatic Hydrocarbons