A Quantitative Assessment of „Through-space”︁ and „Through-bond”︁ Interactions. Application to Semi-empirical SCF Models

The scheme of ‘through-space’ and ‘through-bond’ interaction of (semi)localized orbitals, originally proposed by Hoffmann, is reexamined in terms of SCF many-electron treatments. It is shown that the two types of interaction can be characterized by examining the corresponding off-diagonal matrix elements of the Hartree-Fock matrices of the localized or the symmetry adapted localized orbitals and of the partially diagonalized Hartree-Fock matrices referring to ‘precanonical orbitals’. The procedure outlined is applied to three practical examples using the semiempirical many-electron treatments SPINDO, MINDO/2 and CNDO/2:

• a A reassessment of ‘through-space’ and ‘through-bond’ interaction in norbornadiene indicates, that the latter type of interaction is also of importance for the orbital based mainly on the antisymmetric combination of the localized x-orbitals. The differences in the predictions derived from the three models are critically examined.
• b The competition between ‘through-space’ and ‘through-bond’ interaction in the series of bicyclic dienes from norbornadiene to bicyclo[4.2.2]-dcca-7,9-diene and in cyclohexa-1,4-diene, i. e. their dependence on the dihedral angle UI is reexamined. It is found that the rationalization for the orbital crossing near ω = 130° deduccd from PE. spectroscopic data can not be as simple as originally suggested and that the relay’ orbitals responsible for ‘through-bond interaction affecting both the symmetric and the antisymmetric combination of the π-orbitals extend over the whole CC-σ-system of the six membered ring.
• c ‘Through-bond’ interaction of the two lone pair orbitals in 1,4-diazabicyclo[2.2.2]octane is found to be large for their symmetric and the antisymmetric linear combination.

The analysis quoted, draws attention to some of the dangers involved in using semiempirical treatments for the interpretation of PE. data in terms of Koopmans′ theorem, without due caution.     

Transformation of “living” carbocationic and other polymerizations to controlled/“living” radical polymerization

Transformation of “living” carbocationic polymerization of styrene and isobutene to controlled atom transfer radical polymerization (ATRP) is described and formation of the corresponding AB and ABA block copolymers with styrene (St), methyl methacrylate (MMA, methyl acrylate (MA) and isobornyl acrylate (IBA) was demonstrated. A similar approach was applied to the cationic ring opening polymerization of tetrahydrofuran leading to the AB and ABA block copolymers with St, MMA and MA using ATRP. Site transformation approach was also used for the ring opening metathesis polymerization of norbornene and polycondensation systems using polysulfone as an example. In both cases, AB and ABA block copolymers were efficiently formed with styrene and acrylates.     

Synthesis and reactions of “biginelli-compounds”. Part I

Various reactions of 2-oxo(or thioxo)-1,2,3,4-tetrahydropyrimidine-5-carboxylic acid derivatives (Biginelli-compounds) were investigated. The site of methylation and acylation on 6-methyl-4-phenyl-2-thioxo-1,2,3,4-tetrahydropyrimidine-5-carboxylic acid ethyl ester 1a and its 2-oxo derivative 9a was studied. The synthesis of pyrimido[2,3-b]thiazines and thiazolo[3,2-a]pyrimidines was accomplished by condensation of 1a with 1,3-and 1,2-dielectrophiles. A Dimroth-like rearrangement yielding 6H-1,3-thiazines can be observed when 1a was treated with dimethylformamide and phosphorus oxychloride. The formation of indeno[1,2-d]pyrimidines can be achieved by intramolecular Friedl-Crafts acylation of 9a and 13 , respectively. Finally a route for the preparation of 4,6-disubstituted-pyrimidine-5-carbonitriles is presented, starting with Biginelli-compound 25 .     

Use of heterodifunctional ligands to bridge “early” and “late” transition metals. Construction and chemistry of complexes containing indirectly linked cobalt carbonyl and zirconocene units

Four zirconocene systems, each containing tertiary phosphine functionality indirectly linked to either or both cyclopentadienyl rings, are described. Unlike the phosphinomethylzirconocenes, in which the metal and the phosphine strongly influence each other's basic chemistry, it has been found that a variety of transformations may be carried out at either site on the more indirectly linked systems without interference from the other. Thus reduction and hydrozirconation proceed normally at the Zr center, and quaternization and complexation to a second metal may be achieved at the phosphine. Two “early-late” multimetallic systems containing Zr and Co have been prepared. Reduction and acylation at Co proceed without interference from Zr; however, attempts to generate hydrides at Zr in the bimetallic systems were unsuccessful.     

The Correct Meaning of “Coating Efficiency” vs. the “Utilization of Theoretical Efficiency”

The correct meaning of the the term “utilization of the theoretical efficiency” vs. the “coating efficiency” is explained.     

Professor Carl S. “speed” Marvel

Professor Marvel was one of the great polymer pioneers and innovators. He contributed throughout his lengthy career to every aspect of organic polymer chemistry. His many contributions and activities can be outlined in the following list: education; research; industrial consulting; government; american chemical society; awards; human being I shall discuss each of these in turn.     

Gel-permeation chromatography. V. A study of “overloading effects”

In the calculation of molecular weight averages from GPC chromatograms and in the correction for zone broadening effects, it is assumed that the retention volumes of the individual species are not affected by the presence of the other components in the sample (linear fractionation process). This assumption was tested by the computer comparisons of the chromatograms of mixtures of narrow molecular weight distribution polystyrene standards and the envelopes of the individual chromatograms of the components of the mixtures. Disagreements between experimental and computer synthesized chromatograms were interpreted as non-linear fractionation effects. The investigation covered a range of molecular weights (1.8 × 10⁶ to 2100), molecular weight distributions (binary and seven component mixtures), and sample loadings (2 to 70 mg). Accurate normalizations of raw GPC chromatograms and calculations of molecular weight averages were made possible through an automated GPC apparatus using a high-speed computer for data acquisition and data reduction. It was found that some nonlinear fractionation effects (large disagreement between chromatograms of the mixture and the computed envelopes of the individual chromatograms of the components of the mixture) became more pronounced as sample loading was increased and as the molecular weight distribution of the sample narrows. The nonlinear effect was also found to be sensitive to the molecular weight of the sample.