Incorporating BODIPY fluorophores into tetrakis(arylethynyl)benzenes

Six structural isomers of a tetrakis(arylethynyl)benzene (TAEB) chromophore functionalized with dibutylamine and BODIPY moieties as the corresponding donor and acceptor units were prepared. To evaluate the effectiveness of the donor group, two TAEB molecules and three structurally related bis(arylethynyl)benzene (BAEB) isomers containing only acceptors were also synthesized. The electronic absorption and emission spectra of each series were examined. Additionally, computational studies were employed to corroborate the relative energy levels and gaps present in each series.     

A Practical Application of Linear Programming in the Mining Industry

The paper describes the application of linear programming to the allocation of coking coals from twenty-eight collieries to seven central washeries and blending plants in one N.C.B. area. The problem, which is of the simplex type, is reduced to the transportation form. Some details are given of the production method, implementation of the linear programming model and the follow-up.     

Selection rules and Raman spectrum of a molecule with a degenerate ground state and zero spin-orbit coupling: VCl4

Two interesting features can normally be expected in the Raman spectrum of a molecule with a degenerate electronic ground state (i) the contribution of asymmetric or even antisymmetric tensors to the Raman intensity (ii) lifting of the electronic degeneracy due to Jahn-Teller distortion. The experimental data and discussion on VCl₄, presented here, show that this molecule does not show any deviations in the Raman selection rules. Further, its Raman spectrum closely resembles that of TiCl₄ which also has T_d geometry but a nondegenerate singlet ground state. This suggests the absence of any static Jahn-Teller distortion in VCl₄. However, we have observed a broadening of the ν₂ band of VCl₄ over TiCl₄ and we attribute this to a possible dynamic Jahn-Teller splitting.     

A simple synthesis of 8-(trifluoromethyl)-2,3,5,6,11,12,14,15-octahydro-1H,4H,10H, 13H-diquinolizino[9,9a,1-bc:9′,9a',1-hi] xanthylium perchlorate,an efficient dye

A one-step procedure is described for the preparation of the title compound I, an efficient laser dye operating in the red region.     

Carbon networks based on dehydrobenzoannulenes. 5. Extension of two-dimensional conjugation in graphdiyne nanoarchitectures

[structures: see text] The synthesis and optical properties of a series of multinanometer-sized substructures of the phenyl-diacetylene carbon allotrope, graphdiyne, are described. These molecules are among the largest and most complex annulenic systems yet prepared, with extension of linear conjugation in two-dimensions to over twice that of any previously reported planar macrocycle. The graphdiyne substructures are constructed through convergent syntheses, taking advantage of three key intermediates and silane-protected phenylacetylenes. Intramolecular macrocyclization of alpha,omega-polyyne precursors via Cu-mediated or Pd-catalyzed oxidative homocoupling affords five new graphdiyne "oligomers" possessing two to four fused 18-membered rings. The attempted synthesis of a six-ring analogue is also reported.     

CuCl-induced formation and migration of isoindazolyl carbenoids

Two azo-ene-butadiyne conjugated systems undergo CuCl-mediated cyclization to afford isoindazolyl carbenoids that could be trapped with 2,3-dimethyl-2-butene as [2+1] cycloaddition products. X-ray structure analysis of the resultant cyclopropanes showed that formal migration to the distal carbenoid isomer and subsequent trapping had occurred. The possible CuCl-induced cyclization/migration pathways were explored using density functional theory, which indicated that the reaction most likely occurred via coordination of CuCl to the distal alkyne bond.