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971.
A thymine and acridine conjugate (1), containing a benzylic carbon of thymine and an electron-rich aromatic ring (acridine) within the same molecule, was synthesized. Treatment of 1 with N-bromosuccinimide (NBS) in anhydrous chloroform in the presence of azobisisobutylnitrile produced a dibromo-substituted thymine–acridine conjugate (7) as a major product, in which the bromination was only observed on the acridine ring. Nuclear Overhauser effect (NOE) difference spectroscopy revealed that the actual bromination substitution was on C-2 and C-7 of acridine. Our results suggest that electrophilic aromatic substitution, not the expected benzylic radical reaction, takes place predominantly even when 1 is subjected to the NBS reaction condition, which favors radical processes. In addition, such selectivity is clearly solvent dependent. 相似文献
972.
Dr. Igor E. Soshnikov Dr. Nina V. Semikolenova Prof. Vladimir A. Zakharov Prof. Dr. Heiko M. Möller Franz Ölscher Anna Osichow Dr. Inigo Göttker‐Schnettmann Prof. Dr. Stefan Mecking Prof. Dr. Evgenii P. Talsi Prof. Dr. Konstantin P. Bryliakov 《Chemistry (Weinheim an der Bergstrasse, Germany)》2013,19(34):11409-11417
Formation of Ni–polymeryl propagating species upon the interaction of three salicylaldiminato nickel(II) complexes of the type [(N,O)Ni(CH3)(Py)] (where (N,O)=salicylaldimine ligands, Py=pyridine) with ethylene (C2H4/Ni=10:30) has been studied by 1H and 13C NMR spectroscopy. Typically, the ethylene/catalyst mixtures in [D8]toluene were stored for short periods of time at +60 °C to generate the [(N,O)Ni(polymeryl)] species, then quickly cooled, and the NMR measurements were conducted at ?20 °C. At that temperature, the [(N,O)Ni(polymeryl)] species are stable for days; diffusion 1H NMR measurements provide an estimate of the average length of polymeryl chain (polymeryl=(C2H4)nH, n=6–18). At high ethylene consumptions, the [(N,O)Ni(polymeryl)] intermediates decline, releasing free polymer chains and yielding [(N,O)Ni(Et)(Py)] species, which also further decompose to form the ultimate catalyst degradation product, a paramagnetic [(N,O)2Ni(Py)] complex. In [(N,O)2Ni(Py)], the pyridine ligand is labile (with activation energy for its dissociation of (12.3±0.5) kcal mol?1, ΔH≠298=(11.7±0.5) kcal mol?1, ΔS≠298 =(?7±1) cal K?1 mol?1). Upon the addition of nonpolar solvent (pentane), the pyridine ligand is lost completely to yield the crystals of diamagnetic [(N,O)2Ni] complex. NMR spectroscopic analysis of the polyethylenes formed suggests that the evolution of chain‐propagating species ends up with formation of polyethylene with predominately internal and terminal vinylene groups rather than vinyl groups. 相似文献
973.
Andrew M. Kelly Verena Kaltenhauser Inge Mühlbacher Karl Rametsteiner Harald Kren Christian Slugovc Franz Stelzer Frank Wiesbrock 《Macromolecular bioscience》2013,13(1):116-125
A set of poly(2‐oxazoline)‐derived (co‐)polymers was prepared by microwave‐assisted polymerizations and acid‐mediated hydrolysis and tested for antimicrobial activity in 50 × 50 × 2 mm PP compound plates containing 5 wt% of the polymers. Antimicrobial activity against gram‐negative E. coli and P. aeruginosa as well as C. albicans depended only on the degree of hydrolysis, while antimicrobial activity against gram‐positive S. aureus was only observed for hydrolyzed poly(2‐nonyl‐2‐oxazoline)s. The surface energies of the compound plates compared to pure PP were hardly altered, and the compounds can be considered as alternatives for PP. The presence of the biocide additives at the surface of the PP compound plates could be shown by combined ATR‐IR, zeta potential, and SEM‐EDX measurements. Antimicrobial activity was maintained during double incubation as well as for lowered amounts of the biocide additive of 1% in PP compound plates.
974.
Nghiem Hai Vu Jan‐Erik Damke Tobias Borrmann Lechosław Latos‐Grażyński Franz‐Peter Montforts 《Helvetica chimica acta》2014,97(2):188-196
Azachlorins 7 and 11 , and azahexadehydrocorrin rac‐ 10 are novel structural types of tetrapyrrolic macrocycles. Synthesis of the target structures bearing N‐atoms in the β‐periphery of the macrotetracycles could be achieved by attaching an imidazole moiety 4 to the tricyclic Ni complex rac‐ 5 , followed by cyclization. Depending on the central metal ion of the bilin intermediates rac‐ 6a and rac‐ 6b , chlorin‐ or corrin‐type structures were formed by cyclization. 相似文献
975.
Salah S. Massoud Mark Spell Zadid K. Haq Franz A. Mautner 《Transition Metal Chemistry》2014,39(5):585-591
Four new mononuclear triazido-cobalt(III) complexes [Co(L 1/2/4 )(N3)3] and [Co(L 3 )(N3)3]·CH3CN where L 1 = [(2-pyridyl)-2-ethyl]-(2-pyridylmethyl)-N-methylamine, L 2 = [(2-pyridyl)-2-ethyl]-[6-methyl-(2-pyridylmethyl)]-N-methylamine, L 3 = [(2-pyridyl)-2-ethyl]-[3,5-dimethyl-4-methoxy-(2-pyridylmethyl)]-N-methylamine, and L 4 = [(2-pyridyl)-2-ethyl]-[3,4-dimethoxy-(2-pyridylmethyl)]-N-methylamine, respectively, were synthesized and structurally characterized. The four complexes were characterized by elemental microanalyses, IR and UV–VIS spectroscopy and X-ray single crystal crystallography. The complexes display two strong IR bands over the frequency region 2,020–2,050 cm?1 assigned for the asymmetric stretching frequency, νa(N3) of the coordinated azides indicating facial geometry. The molecular structure determinations of the complexes were in complete agreement with fac-[Co(L)(N3)3] conformation in distorted octahedral Co(III) environment. 相似文献
976.
977.
Roberts JA Franz JA van der Eide EF Walter ED Petersen JL DuBois DL Bullock RM 《Journal of the American Chemical Society》2011,133(37):14593-14603
A series consisting of a tungsten anion, radical, and cation, supported by the N-heterocyclic carbene 1,3-bis(2,4,6-trimethylphenyl)imidazol-2-ylidene (IMes) and spanning formal oxidation states W(0), W(I), and W(II), has been synthesized, isolated, and characterized. Reaction of the hydride CpW(CO)(2)(IMes)H with KH and 18-crown-6 gives the tungsten anion [CpW(CO)(2)(IMes)](-)[K(18-crown-6)](+). Electrochemical oxidation of [CpW(CO)(2)(IMes)](-) in MeCN (0.2 M (n)Bu(4)N(+)PF(6)(-)) is fully reversible (E(1/2) = -1.65 V vs Cp(2)Fe(+?/0)) at all scan rates, indicating that CpW(CO)(2)(IMes)(?) is a persistent radical. Hydride transfer from CpW(CO)(2)(IMes)H to Ph(3)C(+)PF(6)(-) in MeCN affords [cis-CpW(CO)(2)(IMes)(MeCN)](+)PF(6)(-). Comproportionation of [CpW(CO)(2)(IMes)](-) with [CpW(CO)(2)(IMes)(MeCN)](+) gives the 17-electron tungsten radical CpW(CO)(2)(IMes)(?). This complex shows paramagnetically shifted resonances in the (1)H NMR spectrum and has been characterized by IR spectroscopy, low-temperature EPR spectroscopy, and X-ray diffraction. CpW(CO)(2)(IMes)(?) is stable with respect to disproportionation and dimerization. NMR studies of degenerate electron transfer between CpW(CO)(2)(IMes)(?) and [CpW(CO)(2)(IMes)](-) are reported. DFT calculations were carried out on CpW(CO)(2)(IMes)H, as well as on related complexes bearing NHC ligands with N,N' substituents Me (CpW(CO)(2)(IMe)H) or H (CpW(CO)(2)(IH)H) to compare to the experimentally studied IMes complexes with mesityl substituents. These calculations reveal that W-H homolytic bond dissociation energies (BDEs) decrease with increasing steric bulk of the NHC ligand, from 67 to 64 to 63 kcal mol(-1) for CpW(CO)(2)(IH)H, CpW(CO)(2)(IMe)H, and CpW(CO)(2)(IMes)H, respectively. The calculated spin density at W for CpW(CO)(2)(IMes)(?) is 0.63. The W radicals CpW(CO)(2)(IMe)(?) and CpW(CO)(2)(IH)(?) are calculated to form weak W-W bonds. The weakly bonded complexes [CpW(CO)(2)(IMe)](2) and [CpW(CO)(2)(IH)](2) are predicted to have W-W BDEs of 6 and 18 kcal mol(-1), respectively, and to dissociate readily to the W-centered radicals CpW(CO)(2)(IMe)(?) and CpW(CO)(2)(IH)(?). 相似文献
978.
Haas KL Putterman AB White DR Thiele DJ Franz KJ 《Journal of the American Chemical Society》2011,133(12):4427-4437
Cellular acquisition of copper in eukaryotes is primarily accomplished through the Ctr family of copper transport proteins. In both humans and yeast, methionine-rich "Mets" motifs in the amino-terminal extracellular domain of Ctr1 are thought to be responsible for recruitment of copper at the cell surface. Unlike yeast, mammalian Ctr1 also contains extracellular histidine-rich motifs, although a role for these regions in copper uptake has not been explored in detail. Herein, synthetic model peptides containing the first 14 residues of the extracellular domain of human Ctr1 (MDHSHHMGMSYMDS) have been prepared and evaluated for their apparent binding affinity to both Cu(I) and Cu(II). These studies reveal a high affinity Cu(II) binding site (log K = 11.0 ± 0.3 at pH 7.4) at the amino-terminus of the peptide as well as a high affinity Cu(I) site (log K = 10.2 ± 0.2 at pH 7.4) that utilizes adjacent HH residues along with an additional His or Met ligand. These model studies suggest that the histidine domains may play a direct role in copper acquisition from serum copper-binding proteins and in facilitating the reduction of Cu(II) to the active Ctr1 substrate, Cu(I). We tested this hypothesis by expressing a Ctr1 mutant lacking only extracellular histidine residues in Ctr1-knockout mouse embryonic fibroblasts. Results from live cell studies support the hypothesis that extracellular amino-terminal His residues directly participate in the copper transport function of Ctr1. 相似文献
979.
Nicolas R. Ball‐Jones Dr. Joseph J. Badillo Ngon T. Tran Prof. Annaliese K. Franz 《Angewandte Chemie (International ed. in English)》2014,53(36):9462-9465
The first catalytic asymmetric carboannulation with allylsilanes is presented. The enantioselective [3+2] annulation is catalyzed using a scandium(III)/indapybox complex with tetrakis‐[3,5‐bis(trifluoromethyl)phenyl]‐borate (BArF) to enhance catalytic activity and control stereoselectivity. Functionalized cyclopentanes containing a quaternary carbon center are derived from alkylidene oxindole, coumarin, and malonate substrates with high stereoselectivity. The enantioselective 1,4‐conjugate addition and enantioselective lactone formation (by trapping of the β‐silyl carbocation) is also described. 相似文献
980.
In general, Lewis acid catalysts are metal‐based compounds that owe their reactivity to a low‐lying empty orbital. However, one potential Lewis acid that has received negligible attention as a catalyst is the carbocation. We have demonstrated the potential of the carbocation as a highly powerful Lewis acid catalyst for organic reactions. The stable and easily available triphenylmethyl (trityl) cation was found to be a highly efficient catalyst for the Diels–Alder reaction for a range of substrates. Catalyst loadings as low as 500 ppm, excellent yields, and good endo/exo selectivities were achieved. Furthermore, by changing the electronic properties of the substituents on the tritylium ion, the Lewis acidity of the catalyst could be tuned to control the outcome of the reaction. The ability of this carbocation as a Lewis acid catalyst was also further extended to the Michael reaction. 相似文献