Hubbard-type solution in the planar approximation

The Hubbard solution to the Hubbard model showed a non-trivial metal-insulator transition. The value of the one-particle density of states at the Fermi energy in that solution decreased continuously with increasing value of the Hubbard interaction and vanished at a critical value of the interaction. Such a solution is derived from a planar model, as an approximation to the exact construction of the model's one-particle Green function.     

Reduction of Z-2-chlorostilbene with lithium aluminum hydride: evidence for an electron transfer radical mechanism

$\text{Z}$-2-Chlorostilbene undergoes uncatalyzed LiAlH₄ reduction giving phenanthrene and $\text{Z}$-stilbene. An electron transfer radical mechanism is proposed. LiAlH₄ induced isomerization of $\text{Z}$-stilbene produces $\text{E}$-stilbene.     

Pinacol Formation and Reduction of Aromatic Carbonyls with Magnesium–Methanol at Ambient Temperature

A simple and inexpensive procedure for the pinacol formation of aromatic aldehydes and reduction of aromatic ketones to the corresponding alcohols with magnesium in dry methanol at ambient temperature is reported. The pinacol formation and reduction are proposed to be proceeding by SET from magnesium.     

Chemoselective Alkylation of Thiols: A Detailed Investigation of Reactions of Thiols with Halides

Arylthiols, aralkylthiols and alkane thiols can be readily alkylated by alkyl/aralkyl halides in presence of K₂CO₃DMF to yield unsymmetrical sulphides in nearly quantitative yields. 2-Mercaptoethanol gave the thioether chemoselectively.     

Efficient and Green Syntheses of 12-Aryl-2,3,4,12-tetrahydrobenzo[b]xanthene-1,6,11-triones in Water and Task-Specific Ionic Liquid

Facile and convenient one-pot cascade/tandem approaches for the syntheses of privileged medicinal scaffolds, 12-aryl-2,3,4,12-tetrahydrobenzo[b]xanthene-1,6,11-trione derivatives, have been reported under extremely mild reaction conditions using a catalytic amount of H₂SO₄ in water or in the presence of the acidic ionic liquid bmim[HSO₄], which could be recycled.

Supplemental materials are available for this article. Go to the publisher's online edition of Synthetic Communications® to view the free supplemental file.     

Ni Nanoparticles: Mild and Efficient Catalyst for the Chemoselective Synthesis of 2-Arylbenzimidazoles, 2-Arylbenzothiazoles,and Azomethines

A new and efficient method has been developed for the synthesis of biologically significant 2-arylbenzimidazoles, 2-arylbenzothiazoles, and azomethines using recyclable and inexpensive polyvinyl pyrrolidone (PVP)–stabilized Ni nanoparticles in ethylene glycol at room temperature in excellent yields.     

Nickel Boride–Mediated Cleavage of 1,3-Dithiolanes: A Convenient Approach to Reductive Desulfurization

1,3-Dithiolanes are rapidly cleaved by nickel boride, generating corresponding hydrocarbons in excellent yields. The hydrogenolysis is rapid at room temperature and does not require protection from the atmosphere. Mild reaction conditions, simple workup, and good yields of pure products are some of the major advantages of the procedure.     

Facile reductive coupling of benzylic halides with ferrous oxalate dihydrate

Facile reductive coupling of benzylic halides is reported with ferrous oxalate dihydrate in DMF or HMPA under nitrogen atmosphere at 155-160 degrees C. The coupling is proposed to proceed by two successive oxidative additions of benzylic halides to ferrous oxalate to give an intermediate organoiron complex which undergoes concerted dimerization to give the corresponding reductively coupled dimers in high yields.     

New catanionic surfactants, phase stability and synthesis of ultrafine CdS nanoparticles

A systematic study on the water-intake capacity of the microemulsion formed using a catanionic surfactant (synthesized by taking equimolar mixture of acid and amine) with varying hydrocarbon chain length of the acid has been carried out. A decrease in the water-intake capacity with increase in the chain length was observed. Shorter chain length of co-surfactant (1-butanol compared to 1-octanol) led to higher water-intake capacity of microemulsions which may also be attributed to the high hydrophilic-lipophilic balance (HLB) of 1-butanol. Three new microemulsions based on catanionic surfactants have been used to synthesize quantum dots of CdS. The size of CdS quantum dots decreased with increase in chain length of the acid component of the catanionic surfactant.