An Electrochemical Study of Frustrated Lewis Pairs: A Metal-free Route to Hydrogen Oxidation

[Image: see text] Frustrated Lewis pairs have found many applications in the heterolytic activation of H(2) and subsequent hydrogenation of small molecules through delivery of the resulting proton and hydride equivalents. Herein, we describe how H(2) can be preactivated using classical frustrated Lewis pair chemistry and combined with in situ nonaqueous electrochemical oxidation of the resulting borohydride. Our approach allows hydrogen to be cleanly converted into two protons and two electrons in situ, and reduces the potential (the required energetic driving force) for nonaqueous H(2) oxidation by 610 mV (117.7 kJ mol(–1)). This significant energy reduction opens routes to the development of nonaqueous hydrogen energy technology

Development of databases of intelligent expert systems for automatic control of product quality indicators

Abstract Currently existing methods of product quality assessment are far from perfect, since this assessment is carried out in the laboratories of enterprises. Successful solution of this problem is possible when implementing intelligent expert systems for monitoring and forecasting in the flow of product quality indicators using intelligent technologies in the production process. One of the most important components of the expert system is the database. The article deals with the methodological basis for creating databases for building an intelligent expert system for monitoring and forecasting product quality indicators in the production process. Distinctive features of databases are highlighted. The method of database development is investigated and proposed. The main stages of database development are investigated and analyzed. An integrated conceptual model of the domain database of the integrated expert system has been developed. Developed: a tree of database goals, the composition of the main elements of the database system of the intellectual expert system of product quality control. The main phases and stages of designing the database and expert system have been worked out. VAD data flow diagrams are presented. The description of the domain semantics is developed in the form of a system of functional and multi-valued dependencies between attributes of the conceptual model of the domain database. The database architecture has been developed. The developed specialized database of the integrated expert system for monitoring food quality indicators is a single information environment that provides information for automatic control of product quality indicators.</jats:p

A New Route to Annulated Oligothiophenes

A new convenient method for the construction of thiophene-annulated thieno[2,3-b]thiophenes has been proposed. The key step of the method is ring closure of 10H-bisthienodithiocin-10-one by strong bases. The syntheses of two previously unknown annulated oligothiophenes, thieno[2,3-b]thieno[3‘,2‘:4,5]thieno[3,2-d]thiophene (1a) and thieno[3,2-b]thieno[2‘,3‘:4,5]thieno[3,2-d]thiophene (1b), have been described to illustrate the success of the method

A New Route to Annulated Oligothiophenes

A new convenient method for the construction of thiophene-annulated thieno[2,3-b]thiophenes has been proposed. The key step of the method is ring closure of 10H-bisthienodithiocin-10-one by strong bases. The syntheses of two previously unknown annulated oligothiophenes, thieno[2,3-b]thieno[3‘,2‘:4,5]thieno[3,2-d]thiophene (1a) and thieno[3,2-b]thieno[2‘,3‘:4,5]thieno[3,2-d]thiophene (1b), have been described to illustrate the success of the method

Tweezers for Parahydrogen: A Metal-Free Probe of Nonequilibrium Nuclear Spin States of H₂ Molecules

To date, only metal-containing hydrogenation catalysts have been utilized for producing substantial NMR signal enhancements by means of parahydrogen-induced polarization (PHIP). Herein, we show that metal-free compounds known as molecular tweezers are useful in this respect. It is shown that <i>ansa</i>-aminoborane tweezers QCAT provided (20–30)-fold signal enhancements of parahydrogen-originating hydrogens in ¹H NMR spectra. Nuclear polarization transfer from the polarized hydrogens to ¹¹B nuclei leads to a 10-fold enhancement in the ¹¹B NMR spectrum. Moreover, our results indicate that dihydrogen activation by QCAT and CAT tweezers is carried out in a pairwise manner, and PHIP can be used for understanding the activation mechanism in metal-free catalytic systems in general

Reactions of substituted pyridines with electrophilic boranes

Caputo CB, Geier SJ, Winkelhaus D, et al. Reactions of substituted pyridines with electrophilic boranes. Dalton Transactions. 2012;41(7):2131-2139.The lutidine derivative (2,6-Me(2))(4-Bpin)C(5)H(2)N when combined with B(C(6)F(5))(3) yields a frustrated Lewis pair (FLP) which reacts with H(2) to give the salt [(2,6-Me(2))(4-Bpin)C(5)H(2)NH][HB(C(6)F(5))(3)] (1). Similarly 2,2 '-(C(5)H(2)(4,6-Me(2))N)(2) and (4,4 '-(C(5)H(2)(4,6-Me(2))N)(2) were also combined with B(C(6)F(5))(3) and exposed to H(2) to give [(2,2 '-HN(2,6-Me(2))C(5)H(2)C(5)H(2)(4,6-Me(2))N][HB(C(6)F(5))(3)] (2) and [(4,4 '-HN(2,6-Me(2))C(5)H(2)C(5)H(2)(2,6-Me(2))N] [HB(C(6)F(5))(3)] (3), respectively. The mono-pyridine-N-oxide 4,4 '-N(2,6-Me(2))C(5)H(2)C(5)H(2)(2,6-Me(2))NO formed the adduct (4,4 '-N(2,6-Me(2))C(5)H(2)C(5)H(2)(2,6-Me(2))NO)(B(C(6)F(5))(3)) (4) which reacts further with B(C(6)F(5))(3) and H(2) to give [(4,4 '-HN(2,6-Me(2))C(5)H(2)C(5)H(2)(2,6-Me(2)) NO)B(C(6)F(5))(3)] [HB(C(6)F(5))(3)] (5). In a related sense, 2-amino-6-CF(3)-C(5)H(3)N reacts with B(C(6)F(5))(3) to give (C(5)H(3)(6-CF(3))NH)(2-NH(B(C(6)F(5))(3))) (6). Similarly, the species, 2-amino-quinoline, 8-amino-quinoline and 2-hydroxy-6-methyl-pyridine were reacted with B(C(6)F(5))(3) to give the products as (C(9)H(6)NH)(2-NHB(C(6)F(5))(3)) (7), (C(9)H(6)N)(8-NH(2)B(C(6)F(5))(3)) (8) and (C(5)H(3)(6-Me)NH)(2-OB(C(6)F(5))(3)) (9), respectively; while 2-amino-6-picoline, 2-amino-6-CF(3)-pyridine, 2-amino-quinoline, 8-amino-quinoline and 2-hydroxy-6-methyl-pyridine react with ClB(C(6)F(5))(2) to give the species (C(5)H(3)(6-R)NH)(2-NH-(ClB(C(6)F(5))(2))) (R = Me (10), R = CF(3) (11)) (C(9)H(6)NH)(2-NH(ClB(C(6)F(5))(2))) (12), (C(9)H(6)N)(8-NH(2)ClB(C(6)F(5))(2)) (13) and (C(5)H(3)(6-Me)NH)(2-OClB(C(6)F(5))(2)) (14), respectively. In a similar manner, 2-amino-6-picoline and 2-amino-quinoline react with B(C(6)F(5))(2)H to give (C(5)H(3)(6-Me)NH)(2-NH(HB(C(6)F(5))(2))) (15) and (C(9)H(6)NH)(2-NH(HB(C(6)F(5))(2))) (16). The corresponding reaction of 8-amino-quinoline yields (C(9)H(6)N)(8-NHB(C(6)F(5))(2)) (17). In a similar fashion, reaction of 2-amino-6-CF3-pyridine resulted in the formation of (18) formulated as (C(5)H(3)(6-CF(3))N)-(2-NH(B(C(6)F(5))(2)). Finally, treatment of 15 with iPrMgCl gave (C(9)H(6)N)(2-NH(B(C(6)F(5))(2))) (19). Crystallographic studies of 1, 2, 4, 6, 7, 10, 11, 12 and 15 are reported