Synthesis and modification of terrylenediimides as high-performance fluorescent dyes

Two new synthetic approaches to terrylenediimides, highly photostable fluorescent dyes, are described. For the first time terrylenediimide has been synthesised in a straightforward procedure that makes large quantities available. The second route includes an efficient cross-coupling reaction followed by a cyclodehydrogenation. Monofunctionalisation of the imide structure allows terrylenediimides now to be coupled with a variety of compounds, for example, by Suzuki cross-coupling, which can lead to an array of terrylenediimides with new functional groups such as hydroxy, amino, or carboxy groups needed to link up with other molecules. The functionalisation in the bay region is used to tune the properties of terrylenediimides and extend the range of applications, for example, by introducing water solubility. These tetrasubstituted terrylenediimides offer, depending on the substituents used, exciting features such as good solubility in common organic solvents, water solubility, or NIR absorption.     

2-（1,3-Diphenylpropen-1,3-diolato）-1,3,2-（5-formylbenzo）dioxaborol： A ＇Whole-molecule Disorder＇ Crystal Structure

The boron atom in C22H15BO5 is O,O’-chelated by the anions in a tetrahedral geometry, with the planar five-and six-membered chelate rings being orthogonal to each other. The molecule lies on a two-fold rotation axis. The molecule is disordered with respect to another molecule in a 93:7 ratio; the treatment of the ‘whole-molecule disorder’ by employing a large number of restraints is described. Crystal data: C22H15BO5, monoclinic C2/c, a = 17.1804(5), b = 12.9409(4), c = 9.8842(3) , β = 124.832(2)o, V = 1803.82(9) 3 at –173 K.     

Nonlinear Filtering in Rieznnnnifln Manifolds

A general formulation of the nonlinear filtering problem inRiemanman manifolds is given by use of the strong solutionsof the stochastic differential equations for the state and observationprocesses in the orthonormal frame bundles of the state andobservation process manifolds, respectively. A general Bayesformula for the conditional expectation of smooth functionsof the state process is given. This is used to give a directderivation of the Zakai equation for the general problem underconsideration. An example is presented.     

Factorization of proper holomorphic maps on irreducible bounded symmetric domains of rank≥2

We obtain rigidity results on arbitrary proper holomorphic maps F from an irreducible bounded symmetric domain Ω of rank ≥2 into any complex space Z. After lifting to the normalization of the subvariety F (Ω) Z, we prove that F must be the canonical projection map to the quotient space of Ω by a finite group of automorphisms. The approach is along the line of the works of Mok and Tsai by considering radial limits of bounded holomorphic functions derived from F and proving that proper holomorphic maps between bounded symmetric domains preserve certain totally geodesic subdomains. In contrast to the previous works, in general we have to deal with multivalent holomorphic maps for which Fatou’s theorem cannot be applied directly. We bypass the difficulty by devising a limiting process for taking radial limits of correspondences arising from proper holomorphic maps and by elementary estimates allowing us to define distinct univalent branches of the underlying multivalent map on certain subsets. As a consequence of our rigidity result, with the exception of Type-IV domains, any proper holomorphic map f : Ω→ D of Ω onto a bounded convex domain D is necessarily a biholomorphism. In the exceptional case where Ω is a Type-IV domain, either f is a biholomorphism or it is a double cover branched over a totally geodesic submanifold which can be explicitly described.     

Synthesis and structural characterization of five new coordination polymer chain structures using a new,Z-shaped ligand, 2,2′-bis-(4-pyridylethynyl)tolane

Using the new ligand, 2,2-bis-(4-pyridylethynyl)tolane we have synthesized five new coordination polymers: HgBr₂[2,2-bis-(4-pyridylethynyl)tolane] (1), HgI₂[2,2-bis-(4-pyridylethynyl)tolane] (2), Ni(acetylacetonate)₂[2,2-bis-(4-pyridylethynyl)tolane] (3), Zn(acetylacetonate)₂[2,2-bis-(4-pyridylethynyl)tolane] (4), and Cu(hexafluoro acetylacetonate)₂[2,2-bis-(4-pyridylethynyl)tolane]CHCl₃ (5). 2,2-Bis-(4-pyridyl ethynyl)tolane is a rigid ligand with a Z-shape that promotes the formation of zig-zag chains. Compounds 1– 5 were characterized by single crystal X-ray diffraction; and compounds 1– 3 were additionally characterized by IR, elemental analysis, and thermogravimetric analysis. Compound 1 crystallizes in the monoclinic space group C2/c with a = 29.761(3) Å, b = 5.0531(5) Å, c = 16.7823(15) Å, = 104.090(2), V = 2447.9(4) ų, Z = 4. Each mercury is bound to two tolane ligands and two bromine anions, resulting in a tetrahedral coordination environment. Compound 2 crystallizes in the monoclinic space group P2/c, with a = 20.3061(17) Å, b = 5.6303(5) Å, c = 24.5459(19) Å, = 110.338(2), V = 2631.4(4) ų, Z = 4. Here also, each mercury is bound to two tolane ligands and two iodine anions in a tetrahedral coordination environment. The ligand orientation differs in compounds 1 and 2 being trans oriented in 1 and cis oriented in 2. Compound 3 crystallizes in the monoclinic space group P2₁/c with a = 14.5947(14) Å, b = 6.3082(6) Å, c = 18.3939(18) Å, = 112.112(2), V = 1568.9(3) ų, Z = 2. Each nickel is bound to two tolane ligands and two bidentate AcAc anions, resulting in an octahedral coordination environment. Compound 4, which is isostructural with 3, also crystallizes in the monoclinic space group P2₁/c with a = 14.6990(9) Å, b = 6.2724(4) Å, c = 18.6433(11) Å, = 112.8610(10), V = 1583.86(17) ų, Z = 2. Compound 5 crystallizes in the triclinic space group P-1 with a = 6.5487(4) Å, b = 11.6471(7) Å, c = 14.3225(9) Å, = 70.1360(10), = 89.3990(10), = 88.7680(10), V = 1027.18(11) ų, Z = 1. Each copper in 5 is bound to two tolane ligands and two bidentate hfAcAc anions, resulting in an octahedral coordination environment identical to that found in 3 and 4.     

Transfer measurements for the Ti+Ni systems at near barrier energies

Large enhancements have been observed in the sub-barrier fusion cross sections for Ti+Ni systems in our previous studies. Coupled channel calculations incorporating couplings to 2⁺ and 3⁻ states failed to explain these enhancements completely. A possibilty of transfer channels contributing to the residual enhancements had been suggested. In order to investigate the role of relevant transfer channels, measurements of one- and two-nucleon transfer were carried out for ^46,48Ti+⁶¹Ni systems. The present paper gives the results of these studies.     

Nonabsolute Integral on Measure Spaces

We define a Henstock-type integral on measure spaces with metrictopologies, and give an example of a function which is integrablebut whose absolute value is not. 1991 Mathematics Subject Classification26A39, 46G12.     

Water-alcohol Separation by Pervaporation through Zeolite Modified Poly(amidesulfonamide)s (PASAs)

A series of poly(amidesulfonamide)s (PASAs) which have been synthesized in our laboratory possess good membrane fabrication properties^[1]. The potential use of these membrane materials in RO, UF and PV were demonstrated^[2,3]. Reminiscent to the PV performance of other glassy polymers, most of these materials exhibit a fairly high separation factor albeit a permeation flux below 35 g m^-2 h^-1 in the PV separation of aqueous alcohol mixtures. To have a real application prospect in PV, the permeation flux through the membranes has to e further improved. The present work represents our effort to upgrade the separation characteristics of PASAs by blending with inert hydrophilic zeolites. Three types of PASAs (structure shown in Figure 1) were selected to be fabricated by blending different amount of zeolite NaA or NaX. The zeolite filled membranes were characterized by SEM, IR spectroscopy, sorption measurements and wide-angle X-ray diffraction. By adding proper amount of NaA into the polymer casting solutions, the resultant zeolite filled membranes exhibited improvement in both selectivity and permeability in the separation of 10% aqueous solutions of ethanol, propan-l-ol and propan-2-ol, as compared to the zeolite free membrane (Table 1).