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Biographical Memoirs Volume 72 (1997) / Chapter Skim
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LOUIS PLACK HAMMETT
Pages 136-149

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From page 137...
... practice of chemistry and, in particular, changer! the way synthetic organic chemistry is performecI, with enormous practical consequences.
From page 138...
... in 1916 in the micicIle of World War I went to Zurich to work with Hermann Staudinger. On his return to the Uniter!
From page 139...
... with five grancichilciren. Janet also entertained Louis's graduate students en c!
From page 140...
... on the indicator properties of aromatic amines, a scale that measures 100% sulfuric acid as 10~° times as strong (that is, ten billion times as strong) as 10% acicI, en c!
From page 141...
... 100% sulfuric acid into true superaciclic merlin, such as fuming sulfuric acicI, or solutions of HF in BF3. George Olah won the 1995 Nobel Prize in chemistry for his demonstration of the catalytic effects of such superacic!
From page 142...
... Chemists had long realized that reactions with large negative free energies may nevertheless be extremely slow. For example, the equilibrium position for Egyptian sarcophagi en c!
From page 143...
... aromatic compounds presumably means that here steric effects complicate what are otherwise resonance en c! electrostatic ones.
From page 144...
... an Explosives Research Laboratory outside Pittsburgh at Bruceton, Pennsylvania, on the site of the Bureau of Mines with George Kistiakowsky as director en c! Hammett as associate director.
From page 145...
... imaginatively. The civil service employees of the Bureau of Mines were left behinc!
From page 146...
... in the archives of the National Academy of Sciences. In 1951, when he was finally appointed chairman, he supervised the buildup of the Chemistry Department at Columbia en c!
From page 147...
... Autobiographical notes. Files of the National Academy of Sciences.
From page 148...
... Paul. The relation between the rates of some acid catalyzed reactions and the acidity function, Ho.
From page 149...
... Cryoscopic study on bases in sulfuric acid. The ionization of diorthosubstituted benzoic acids.


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