325,764 research outputs found
Catalytic Applications of Pyridine-Containing Macrocyclic Complexes
Polyazamacrocycles are a common class of macrocyclic compounds, utilized across a number of fields, including, but not limited to, catalysis, selective metal recovery and recycling, therapy and diagnosis, and materials and sensors.1 Worth of note is their ability to form stable complexes with a plethora of both transition, especially late, and lanthanide metal cations.2 Deviation of the macrocycle donor atoms from planarity often leads to rather uncommon oxidation states.3 Both the thermodynamic properties and the complexation kinetics are strongly affected by the introduction of a pyridine moiety into the skeleton of polyazamacrocycles by increasing the conformational rigidity and tuning the basicity.4 Pyridine-containing ligands engender great interest due to various potential field of applications. They have been successfully employed in biology, Magnetic Resonance Imaging, molecular recognition, supramolecular chemistry and self-assembly, molecular machines and mechanically interlocked architectures.5 In this lecture, I will provide a perspective on the catalytic applications of metal complexes of pyridine-containing macrocyclic ligands (Pc-L’s) which have been studied in our group (Figure), with a focus interest on the structural features relevant to catalysis.6 The increased conformational rigidity imposed by the pyridine ring allowed for the isolation and characterization of metal complexes which showed a rich coordination chemistry.7 The very different conformations accessible upon coordination and the easy tuneable synthesis of the macrocyclic ligands have been exploited in stereoselective syntheses.8
References:
1 L. F. Lindoy, G. V. Meehan, I. M. Vasilescu, H. J. Kim, J.-E. Lee, S. S. Lee, Coord. Chem. Rev. 2010, 254, 1713.
2 T. Ren, Chem. Commun. 2016, 52, 3271.
3 A. Casitas, X. Ribas, Chem. Sci. 2013, 4, 2301.
4 K. M. Lincoln, M. E. Offutt, T. D. Hayden, R. E. Saunders, K. N. Green, Inorg. Chem. 2014, 53, 1406.
5 M. Rezaeivala, H. Keypour, Coord. Chem. Rev. 2014, 280, 203.
6 B. Castano, S. Guidone, E. Gallo, F. Ragaini, N. Casati, P. Macchi, M. Sisti, A. Caselli, Dalton Trans. 2013, 42, 2451.
7 a) G. Tseberlidis, M. Dell'Acqua, D. Valcarenghi, E. Gallo, E. Rossi, G. Abbiati, A. Caselli, RSC Adv. 2016, 6, 97404; b) T. Pedrazzini, P. Pirovano, M. Dell'Acqua, F. Ragaini, P. Illiano, P. Macchi, G. Abbiati, A. Caselli, Eur. J. Inorg. Chem. 2015, 2015, 5089.
8 a) M. Dell’Acqua, B. Castano, C. Cecchini, T. Pedrazzini, V. Pirovano, E. Rossi, A. Caselli, G. Abbiati, J. Org. Chem. 2014, 79, 3494; b) M. Trose, M. Dell’Acqua, T. Pedrazzini, V. Pirovano, E. Gallo, E. Rossi, A. Caselli, G. Abbiati, J. Org. Chem. 2014, 79, 7311; c) B. Castano, E. Gallo, D. J. Cole-Hamilton, V. Dal Santo, R. Psaro, A. Caselli, Green Chem. 2014, 16, 3202
Designing new Ligands: Catalytic Applications of Pyridine-Containing Macrocyclic Complexes
The introduction of a pyridine moiety into the skeleton of a polyazamacrocyclic ligand affects both the thermodynamic properties and the coordination kinetics of the resulting metal complexes. These features have engender a great interest in the scientific community and the applications of pyridine-containing macrocyclic ligands ranges from biology to supramolecular chemistry, encompassing MRI, molecular recognitions, materials and catalysis. In this lecture, I will provide a perspective on the catalytic applications of metal complexes of pyridine-containing macrocyclic ligands (Pc-L’s) which have been studied in our group (Figure 1), with a focus interest on the structural features relevant to catalysis.1 The increased conformational rigidity imposed by the pyridine ring allowed for the isolation and characterization of metal complexes which show a rich coordination chemistry.2 The very different conformations accessible upon coordination and the easy tuneable synthesis of the macrocyclic ligands have been exploited in stereoselective syntheses.3
References
1 B. Castano, S. Guidone, E. Gallo, F. Ragaini, N. Casati, P. Macchi, M. Sisti, A. Caselli, Dalton Trans. 2013, 42, 2451.
2 a) G. Tseberlidis, M. Dell'Acqua, D. Valcarenghi, E. Gallo, E. Rossi, G. Abbiati, A. Caselli, RSC Adv. 2016, 6, 97404; b) T. Pedrazzini, P. Pirovano, M. Dell'Acqua, F. Ragaini, P. Illiano, P. Macchi, G. Abbiati, A. Caselli, Eur. J. Inorg. Chem. 2015, 2015, 5089.
3 a) M. Dell’Acqua, B. Castano, C. Cecchini, T. Pedrazzini, V. Pirovano, E. Rossi, A. Caselli, G. Abbiati, J. Org. Chem. 2014, 79, 3494; b) M. Trose, M. Dell’Acqua, T. Pedrazzini, V. Pirovano, E. Gallo, E. Rossi, A. Caselli, G. Abbiati, J. Org. Chem. 2014, 79, 7311; c) B. Castano, E. Gallo, D. J. Cole-Hamilton, V. Dal Santo, R. Psaro, A. Caselli, Green Chem. 2014, 16, 3202
Formulas for multi-parameter classes of Kazhdan-Lusztig polynomials for S(n)
We give explicit formulas for several classes of Kazhdan-Lusztig polynomials of the symmetric group which are related to others already considered in the literature. In particular, we generalize two theorems of Brenti and Simion [Explicit formulae for some classes of Kazhdan-Lusztig polynomials, J. Algebraic Combin. 11 (2000), 187-196], we prove an unpublished conjecture of Brenti, and we treat the case missing in Theorem 4.8 of [F. Caselli, Proof of two conjectures of Brenti and Simion on Kazhdan-Lusztig polynomials, J. Algebraic Combin. 18 (2003), 171-187]
Le best practice internazionali: il caso delle SBIC - Small Bsuiness Investment Company americane
Il lavoro sviluppa un'analisi delle caratteristiche del mercato delle SBIC americane, valutandone l'impatto sotto il profilo della performance degli investimenti effettuati. L'analisi descrive per la prima volta il frenomeno, tracciandone l'evoluzione a partire dal 1958, anno in cui sono state introdotte nell'ordinamento americano per sostenere la crescita del private equity
Selective oxidation of alkenes by H2O2 catalysed by well-defined [Iron(III)(Pyridine-Containing Ligand)] complexes
The introduction of a pyridine moiety into the skeleton of a polyazamacrocyclic ligand affects both thermodynamic properties and coordination kinetics of the resulting metal complexes (1). These features have engendered a great interest of the scientific community in recent years. The applications of pyridine-containing macrocyclic ligands ranges from biology to supramolecular chemistry, encompassing MRI, molecular recognitions, materials and catalysis. Much of the efforts in the use of macrocyclic pyridine containing ligands have been devoted to the study of catalytic oxidation reactions. We report here the synthesis and characterization of [Fe(III)Pc-L’s)] complexes (Pc-L = Pyiridine-Containing Ligand) and their catalytic applications in alkene epoxidation or cis-dihydroxylation reactions using H2O2 as the terminal oxidant under mild conditions (Figure). Depending on the anion employed for the synthesis of the iron(III) metal complex, we observed a completely reversed selectivity. When X = OTf, a selective cis-dihydroxylation reaction was observed. On the other hand, employing X = Cl, we obtained the epoxide as the major product (traces of aldehyde were observed at very high conversions). It should be pointed out that under otherwise identical reaction conditions, using FeCl3·6H2O as catalyst in the absence of the ligand, no reaction was observed.
References:
1 a) B. Castano, S. Guidone, E. Gallo, F. Ragaini, N. Casati, P. Macchi, M. Sisti, A. Caselli, Dalton Trans. 2013, 42, 2451; b) G. Tseberlidis, M. Dell'Acqua, D. Valcarenghi, E. Gallo, E. Rossi, G. Abbiati, A. Caselli, RSC Adv. 2016, 6, 97404; c) T. Pedrazzini, P. Pirovano, M. Dell'Acqua, F. Ragaini, P. Illiano, P. Macchi, G. Abbiati, A. Caselli, Eur. J. Inorg. Chem. 2015, 2015, 5089
Amination of C-H Bonds by Metal Porphyrins Catalysed Nitrene Transfer Reaction
The biological and pharmaceutical activities of organonitrogen compounds prompted the scientific community to develop new methods for the direct and selective C-N bond formation, working within restricted financial parameters and environmentally friendly requirements.In the last few years we have reported on the catalytic activity of metal porphyrin complexes in a wide range of reactions, such as olefin epoxidation,1 hydrocarbon amination and olefin aziridination. For these last reactions arylazides, a versatile class of starting material, was employed as atom-efficient aminating agents.2 ArN3 generate a nitrene functionality “ArN” and the eco-friendly molecular nitrogen is the only side product.
The selective insertion of “ArN” into C–H bonds of benzylic substrates or olefins yields benzylic amines, benzylic imines or allylic amines. To clarify the mechanism of the C-H amination reactions, the ruthenium bis-imido porphyrin complex (1) was isolated and characterised by X-ray analysis.
The role of 1 in catalytic nitrene insertions into C H bonds was studied in the reaction of ArN3 with several hydrocarbons proving that 1 is an active reaction intermediate. It also appears to have equilibrium between stability and reactivity.3 To the best of our knowledge, complex 1 is the first structurally characterized bis-imido porphyrin complex that shows a good catalytic activity in this class of reactions.
References: [1] S. Fantauzzi, E. Gallo, E. Rose, N. Raoul, A. Caselli, S. Issa, F. Ragaini, S. Cenini, Organometallics , 2008, 27, 6143; [2] For a review see: S. Fantauzzi, A. Caselli and E. Gallo, Dalton Trans., 2009, 5434; [3] S. Fantauzzi, E. Gallo, A. Caselli, F. Ragaini, N. Casati, P. Macchi and S. Cenini Chem. Commun., 2009, 3952–395
“Competitive models of corporate banking and venture capital”
Venture Capital. A Euro-System Approach covers a wide spectrum of topics: it investigates the way venture capital really works, the relations between venture capital, corporate banking and stock exchanges, market trends in Europe and the US, legal issues related to the creation of venture capital firms and closed end funds, and finally regulatory and economic policy issues. The book is based on a strong link between a rigorous methodological approach and real world best practices of venture capitalists - thanks to a team of contributors formed by both academics and professionals of different fields (venture capitalists, financial analysts, regulators, stock exchange executives)
Pierre Caselli, bust shot
Serves America - Pierre Caselli of 3317 University Drive, who came to the United States two years ago from France, Monday enlisted in the U. S. Air Force after he was classified 1-A by the Army. Caselli will get basic training in San Antonio. He attended Texas Christian University (TCU) and had been assistant import-export manager for Kimbell Milling Company here.https://mavmatrix.uta.edu/specialcollections_startelegram1950s/13879/thumbnail.jp
“Structured Leasing Deals"
The paper faces the issue of deal making through structured leasing solutio
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