Nal

Bardeen C J, Che J, WIson K R, Yakovlev V V, Cong P, Kohler B, Krause J L and Messina M 1997 Quantum control of Nal photodissociation reaction product states by ultrafast tailored light pulses J. Phys. Chem. A 101 3815-22... 

One of the early examples for kinetic studies on the femtosecond time scale is the photochemical predissociation of Nal [74] ... 

The experiment is illustrated in figure B2.5.9. The initial pump pulse generates a localized wavepacket in the first excited state of Nal, which evolves with time. The potential well in the state is the result of an avoided crossing with the ground state. Every time the wavepacket passes this region, part of it crosses to the lower surface before the remainder is reflected at the outer wall of the potential. The crossing leads to... 

Figure B2.5.10. LIF signal of free Na atoms produced in the photodissociation of Nal. t - q is the delay between the photolysis pulse (at L) and the probe pulse. Adapted from [111].

However, th ese alternative methods can be on ly applied to certain elements. For example, the projected CXDO/IXDOi may be used only for molecular system s with atom ic n iiin bers less than or ct nal to IS (Ari. Elements beyond IS are not available in the projected CXDO/IXD(f initial guess. 

C and T Lengauer 2000. Computational Methods for the Structural Alignment of Molecules. nal of Computer-Aided Molecular Design 14 215-232. 

METHOD 2 Speed chemists have used hydroiodic acid (HI) for years to reduce ephedrine to meth. So when the government placed HI on the restricted list, speed chemists took to making the HI themselves. One of the ways they used was to make Hi in DMSO (dimethylsulfoxide, a common solvent) by reacting Nal or Kl with sulfuric acid. This a standard way to make both HBr or Hi in water (see the Chemicals section of this book) except these speed chemists were using the non-aqueous solvent DMSO instead of water. 

One need not inhibit oneself by using HBr. One can use Nal or Kl to make HI which is even better than HBr in any of these recipes. Iodine adds much better and swaps out with the amines much better. Yield are much higher The other thing to notice is that reaction carries itself out in DMSO. Seems logical to believe that one could bubble their HBr gasses into this solvent instead of acetic acid. 

MejSiCI - Nal - CH3CN as an Efficient and Practical Reducing Agent for Benzoic Alcohols. A typical procedure for the present reduction is as follows To a mixture of MejSiCI (1.54 ml, 12 mmol), Nal (1.8 g, 12 mmol), and acetonitrile (0.6 ml, 12 mmol) was added a solution of 1-phenylethanol (244 mg, 2 mmol) in hexane (2 ml). The mixture was stirred for 24 h at room temperature. Dilution with water, extraction with ether and subsequent isolation process gave ethylbenzene (158 mg) with sufficient purity in 75% yield. ... 

Regioselectivity of C—C double bond formation can also be achieved in the reductiv or oxidative elimination of two functional groups from adjacent carbon atoms. Well estab llshed methods in synthesis include the reductive cleavage of cyclic thionocarbonates derivec from glycols (E.J. Corey, 1968 C W. Hartmann, 1972), the reduction of epoxides with Zn/Nal or of dihalides with metals, organometallic compounds, or Nal/acetone (seep.lS6f), and the oxidative decarboxylation of 1,2-dicarboxylic acids (C.A. Grob, 1958 S. Masamune, 1966 R.A. Sheldon, 1972) or their r-butyl peresters (E.N. Cain, 1969). 

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