Pauling, Linus, 168 elements

Linus Pauling, "The Nature of the Chemical Bond. III. The Transition from One Extreme Bond Type to Another," JACS 54 (1932) 981003 Linus Pauling, "Interatomic Distances in Covalent Molecules and Resonance between Two or More Lewis Electronic Structures," Proc.NAS 18 (1932) 293297 Linus Pauling, "The Calculation of Matrix Element for the Lewis Electronic Structure of Molecules,"... 

An important element in the three-dimensional structure of a protein is the secondary structure. The secondary structure results from the formation of hydrogen bonds between the—N—H groups and the carbonyl (C O) groups of the peptide bonds —N—H 0=C. There are two basic ways to do this. We can form a helix or we can form a sheet. The great American chemist Linus Pauling won the Nobel Prize in Chemistry in 1954 for the elucidation of these structures. 

Around 1935, the American chemist Linus Pauling developed a scale of electronegativity to describe the attraction an element has for electrons in a chemical bond. The values in Figure 5-13 are higher for elements that more strongly attract electrons, which increase the likelihood of a negative partial charge on that atom. 

The structures of the basic building blocks of the architecture of proteins were determined by Linus Pauling and R. B. Corey many years before the solution of the structures of globular proteins.13 They solved the structures of crystalline small peptides to find the dimensions and geometry of the peptide bond. Then, by constructing very precise models, they found structures that could fit the x-ray diffraction patterns of fibrous proteins. The diffraction patterns of fibers do not consist of the lattice of points found from crystals, but a series of lines corresponding to the repeat distances between constantly recurring elements of structure. 

Hence, some hetero-atomic bonds must be considerably stronger than the homo-atomic bonds in the elements. Linus Pauling considered this tendency to be so fundamental that the defined the thermochemical electronegativity x from the relation of bond strengths (AH0 values)/ for dissociation to gaseous atoms... 

Spectroscopy and the electron theory of valence provided valuable support for one another. Together, they took our understanding of the nature of chemical elements to a new level, where chemical behavior and chemical structure could both be interpreted in terms of the number and disposition of electrons in the atoms of any given element. At least, the simplified model of atomic orbitals brilliantly developed by Linus Pauling enabled him to explain and predict a great deal of chemistry, in terms of bonds and structures. 

This was developed by Linus Pauling in 1931 and was the first quantum-based model of bonding. It is based on the premise that if the atomic s, p, and d orbitals occupied by the valence electrons of adjacent atoms are combined in a suitable way, the hybrid orbitals that result will have the character and directional properties that are consistent with the bonding pattern in the molecule. The rules for bringing about these combinations turn out to be remarkably simple, so once they were worked out it became possible to use this model to predict the bonding behavior in a wide variety of molecules. The hybrid orbital model is most usefully applied to the p-block elements the first two rows of the periodic table, and is especially important in organic chemistry see Page 37. 

A review of the unsynchronized-resonating-covalent-bond theory of metals in presented. Key concepts, such as unsynchronous resonance, hypoelectronic elements, buffer elements, and hyperelectronic elements, are discussed in detail. Application of the theory is discussed for such things as the atomic volume of the constituents in alloys, the structure of boron, and superconductivity. These ideas represent Linus Pauling s understanding of the nature of the chemical bond in metals, alloys, and intermetallic compounds. 

The application of Walter Heftier and Fritz London s valence bond theory was the first description of the binding forces in the H2 molecule, the simplest neutral molecule. Linus Pauling and John Slater later extended the principles to larger molecules. The key element in their proposal was the synthesis of a bonding wavefunction resulting from a combination of atomic orbitals that link the two atoms in a bond. It was hugely important that this localized approach concurred with the Lewis dot model. For the simplest neutral molecule, H2, the Hamiltonian operator may be written... 

Lewis published these ideas in his 1923 book Valence and the Structure of Atoms and Molecules, and they were widely taken up and developed in the U.S.A. and Europe, for example, by N. V. Sidgwick at Oxford, whose Electronic Theory of Valency appeared in 1927. The Nobel Prize in Chemistry was left unfilled in 1919, 1924 and 1933 for lack of candidates of suitable stature, and Lewis would have been an appropriate candidate for any of these years. In fact, he was nominated for a Nobel Prize by the inorganic chemist and historian of chemistry, J. R. Partington (1886-1965) at the University of London. For the first half-century after the award of the first Nobel Prize in Chemistry to van t Hoff in 1901, the chemistry prize went to those who had discovered or characterised new chemical elements, new physico-chemical principles, new chemical reactions, or had elucidated the structure and accomplished the synthesis of natural products. The first award for research into the nature of the chemical bond and its application to the elucidation of the structure of complex substances went in 1954 to Linus Pauling at Caltech. 

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