The Quantum Mechanics of Chemical Reactions Involving Conjugate Double Bonds

1933 ◽  
Vol 1 (8) ◽  
pp. 586-592 ◽  
Author(s):  
Henry Eyring ◽  
Albert Sherman ◽  
George E. Kimball
Author(s):  
Prajakta U. Kulkarni ◽  
Harshil Shah ◽  
Vivek K. Vyas

: Quantum mechanics (QM) is physics based theory which explains the physical properties of nature at the level of atoms and sub-atoms. Molecular mechanics (MM) construct molecular systems through the use of classical mechanics. So, hybrid quantum mechanics and molecular mechanics (QM/MM) when combined together can act as computer-based methods which can be used to calculate structure and property data of molecular structures. Hybrid QM/MM combines the strengths of QM with accuracy and MM with speed. QM/MM simulation can also be applied for the study of chemical process in solutions as well as in the proteins, and has a great scope in structure-based drug design (CADD) and discovery. Hybrid QM/MM also applied to HTS, to derive QSAR models and due to availability of many protein crystal structures; it has a great role in computational chemistry, especially in structure- and fragment-based drug design. Fused QM/MM simulations have been developed as a widespread method to explore chemical reactions in condensed phases. In QM/MM simulations, the quantum chemistry theory is used to treat the space in which the chemical reactions occur; however the rest is defined through molecular mechanics force field (MMFF). In this review, we have extensively reviewed recent literature pertaining to the use and applications of hybrid QM/MM simulations for ligand and structure-based computational methods for the design and discovery of therapeutic agents.


Author(s):  
Tom McLeish

‘Sliminess and stickiness’ examines the molecular origin of ‘stickiness’. It details Hermann Staudinger’s research on ‘double bonds’ and ‘macromolecules’. Understanding the unorthodox properties of the polymer liquid and gel state turned out to be one of the first successes of soft matter science. Staudinger faced a challenge: how much space would a polymer molecule occupy when in solution? Many of the mathematical techniques that had been developed to deal with the quantum mechanics of electrons, photons, and their interaction in solids could be translated into tools for solving polymer problems such as this one. The properties of rubber, and the sticky sliminess of rubbery liquids, are topics which relate to the notion of stickiness.


1938 ◽  
Vol 11 (1) ◽  
pp. 107-130
Author(s):  
W. K. Lewis ◽  
Lombard Squires ◽  
Robert D. Nutting

Abstract THAT vulcanization of rubber with sulfur always involves a chemical reaction consisting in the addition of sulfur to the double bonds of the rubber molecule has been conclusively established (18, 28). The facts indicate that this addition of sulfur to rubber is an irreversible reaction (31). The temperature coefficient of the reaction is high, increasing about 2.65 fold per 10° C. at ordinary curing temperatures (31). Furthermore, the reaction is apparently exothermic (4, 24). It is noteworthy that catalysts are apparently necessary, since synthetic rubbers prepared from pure materials add sulfur slowly, if at all. The proteins and perhaps the resins in natural rubber undoubtedly serve as accelerators. The curves for combined sulfur vs. time of cure for typical mixes are shown in Figures 1 and 2. Figure 1 is taken from the data of Kratz and Flower (16); the composition and temperature of cure for this mix are shown in Cranor's Table I (9). Figure 2, curve 1, is from Table I of Eaton and Day (10), and curve 2 from data obtained in this laboratory (27, Table I). Superficial inspection of these curves shows extraordinary divergence of type. Figure 1 is a typical fadeaway curve, characteristic of most chemical reactions, where the reaction rate decreases with decreasing concentration of the reacting materials. Curve 1, Figure 2, is an entirely different type, where the rate of sulfur addition is constant until nearly 70 per cent of the initial sulfur has reacted. Curve 2, Figure 2, shows even more complex behavior. Again the rate is constant in the initial portions of the cure. However, following this period, the rate increases markedly but later falls off, approaching zero, to give an S-shaped eurve.


1986 ◽  
Vol 64 (8) ◽  
pp. 1553-1559 ◽  
Author(s):  
Karl Griesbaum ◽  
Ashis R. Bandyopadhyay ◽  
Martin Meister

The chlorodienes (E)-4-chloro-3-methyl-1,3-hexadiene (5a), (E)- and (Z)-4-chloro-2,3-dimethyl-1,3-hexadiene (5b/6b), (E,E)-5-chloro-4-methyl-2,4-heptadiene (5c), (4E)- and (4Z)-5-chloro-3,4-dimethyl-2,4-heptadiene (5d/6d), chloroprene (11a), and 2-chloro-3-methyl-1,3-butadiene (11b) are selectively ozonized at the non-chlorinated double bonds to give the corresponding monoozonides 7, 8, and 12. Further ozonolyses of the monoozonides of 5b and of 11b in methanol as well as epoxidation of the monoozonide of 5b and subsequent reaction of the resulting chloroepoxide with AgBF4 are described.


1946 ◽  
Vol 19 (3) ◽  
pp. 534-545
Author(s):  
Max H. Keck ◽  
La Verne E. Cheyney

Abstract In conclusion, the data presented here indicate that two types of chemical reactions take place during the vulcanization of Buna-S stocks of a specific type: (1) a combination with sulfur, which may or may not involve the double bonds in the polymer, and which may be similar in character to the primary vulcanization reaction of natural rubber; (2) a second reaction, presumably polymerization, which accompanies the first and is related to and possibly initiated by it, and which continues on over cure.


1942 ◽  
Vol 15 (3) ◽  
pp. 560-571
Author(s):  
E. A. Hauser ◽  
M. C. Sze

Abstract From the preceding discussion the following conclusions may be drawn: A. Vulcanization with Sulfur in General 1. Vulcanization with sulfur is fundamentally a chemical change involving activated sulfur and organic double bonds. 2. Sulfur must decompose from S8 (in the form of an eight-membered ring) to smaller molecular units, perhaps to S2 and S1 before it can be activated and react. 3. The ratio of atoms of sulfur combined to the number of double bonds lost is not restricted to one atom of sulfur for each double bond, but may have other values, which depend on the conditions and the reactions involved. B. Factice Formation 1. The rate of reaction of sulfur with tung and linseed oils is greatly influenced by small proportions of such agents as zinc oxide and mercaptobenzothiazole. 2. Combination of sulfur with the conjugated double bonds of the eleostearic acid in tung oil takes place at the terminal carbon atoms of the conjugated system, giving a typical 1,6-addition. 3. The following possible chemical reactions explain adequately the process of factice formation from tung and lineseed oil. Under different conditions different reactions predominate.


Author(s):  
Erik Rohloff ◽  
Dominik Rudolph ◽  
Onno Strolka ◽  
Irmgard Frank

Is a classical description of nuclear motion sufficient when describing chemical reactions? The present paper investigates some phenomena that were previously attributed to nuclear quantum effects. The aim is to show that these phenomena can be modelled with traditional Car-Parrinello molecular dynamics, that is, with a method which treats nuclear motion classically. We find that no additional paradigm is needed for describing chemical reactions. The special reactivity observed for carbenes can be attributed to the special environment represented by a noble gas matrix. Also the infrared spectrum of porphycene is perfectly modelled by traditional Car-Parrinello molecular dynamics. If no more convincing examples are produced, one will stick to deterministic quantum mechanics, as it is the simpler theory which, in addition, is free of paradoxa.


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