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Photoassisted oxygenation of alkane catalyzed by ruthenium complexes using 2,6-dichloropyridine N-oxide under visible light irradiationElectronic supplementary information (ESI) available: syntheses of the complexes, crystallographic data of complex 4 (Table S-1), 1H NMR spectra before and after irradiation (Fig. S-1, S-2, S-3, S-5), UV-vis spectral change (Fig. S-4, S-6). See http://www.rsc.org/suppdata/cc/b3/b316970g/

✍ Scribed by Yamaguchi, Motowo; Kumano, Takashi; Masui, Dai; Yamagishi, Takamichi

Book ID: 111881985
Publisher: Royal Society of Chemistry
Year: 2004
Tongue: English
Weight: 117 KB
Volume: 7
Category: Article
ISSN: 1359-7345
DOI: 10.1039/b316970g

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📜 SIMILAR VOLUMES

Acid?base equilibria of various oxidatio

Acid?base equilibria of various oxidation states of aqua?ruthenium complexes with 1,10-phenanthroline-5,6-dione in aqueous mediaElectronic supplementary information (ESI) available: 1H NMR spectrum of [1](ClO4)2 (Fig. S1), Cyclic voltammogram of [1](ClO4)2 (Fig. S2), pH dependent UV-vis spectra of [2](ClO4)2 (Fig. S3), and cyclic voltammograms of [2](ClO4)2 (Fig. S4). See http://www.rsc.org/suppdata/dt/b3/b312310c/

✍ Fujihara, Tetsuaki; Wada, Tohru; Tanaka, Koji 📂 Article 📅 2004 🏛 Royal Society of Chemistry 🌐 English ⚖ 273 KB

Synthesis, characterization and luminesc

Synthesis, characterization and luminescence properties of homoleptic platinum(ii) acetylide complexesElectronic supplementary information (ESI) available: Experimental section. Fig. S1: Molecular structure of the anion of 6. Fig. S2: Emission spectra of complex 7. Fig. S3: Excitation and emission spectra of complex 3. Fig. S4: Emission spectra of complex 6. Table S1: Population analysis (%) for the anion of complex 6. Table S2: Emission and excitation spectral data for complexes 1?4 and 6. Table S3: TD-DFT RPA singlet excitation calculations for the anion of complex 6. See http://www.rsc.org/suppdata/dt/b3/b308291a/

✍ Benito, Jos�; Berenguer, Jes�s R.; Forni�s, Juan; Gil, Bel�n; G�mez, Julio; Lali 📂 Article 📅 2003 🏛 Royal Society of Chemistry 🌐 English ⚖ 230 KB

Aerial oxidation of primary alcohols and

Aerial oxidation of primary alcohols and amines catalyzed by Cu(ii) complexes of 2,2?-selenobis(4,6-di-tert-butylphenol) providing [O,Se,O]-donor atomsElectronic supplementary information (ESI) available: Molecular structures of H2LSe (Fig. S1), complex 2 [CuLSe(Et2NH)] (Fig. S2), complex 5 [(LSe)2(HLSe)Cu3(�2-OH)(CH3CN)] (Fig. S3) and EPR spectra for complexes 1, 4 and 5 with their simulations (Figs. S4?S7). Tables S1 and S2 list the bond lengths and angles for H2LSe and complex 5, respectively. See http://www.rsc.org/suppdata/dt/b4/b403953j/

✍ Paine, Tapan K.; Weyherm�ller, Thomas; Wieghardt, Karl; Chaudhuri, Phalguni 📂 Article 📅 2004 🏛 Royal Society of Chemistry 🌐 English ⚖ 485 KB

Mononuclear nitrogen/sulfur-ligated coba

Mononuclear nitrogen/sulfur-ligated cobalt(ii) methoxide complexes: Structural, EPR, paramagnetic 1H NMR, and electrochemical investigationsElectronic supplementary information (ESI) available: Experimental details, and Figs. S1 (EPR spectra of 1 and 2 in MeOH soln.), S2 and S4 (1H NMR spectra of 1 in CD3CN), S3 and S5 (1H NMR spectra of 2 in CD3CN), S6 (cyclic voltammetry of 1 and 2) and Table S1 (1H NMR features of 1 and 2 in CD3CN at 302 K). See http://www.rsc.org/suppdata/dt/b4/b408177c/

✍ Tubbs, Kyle J.; Szajna, Ewa; Bennett, Brian; Halfen, Jason A.; Watkins, Rex W.; 📂 Article 📅 2004 🏛 Royal Society of Chemistry 🌐 English ⚖ 276 KB

Dimetallic complexes of acyclic pyridine

Dimetallic complexes of acyclic pyridine-armed ligands derived from 3,6-diformylpyridazineElectronic supplementary information (ESI) available: Figs. S1?3: NMR spectra. Fig. S4: Line diagram of the least squares fit of the nitrogen atoms of L and bridging azide atoms of the two independent molecules of 7 in the asymmetric unit. Fig. S5?7: cyclic voltammetric data. Fig. S8?11: Variable temperature susceptibility and magnetic moment data. See http://www.rsc.org/suppdata/dt/b4/b403131h/

✍ Plieger, Paul G.; Downard, Alison J.; Moubaraki, Boujemaa; Murray, Keith S.; Bro 📂 Article 📅 2004 🏛 Royal Society of Chemistry 🌐 English ⚖ 423 KB

1H-1,3-Diazepines, 5H-1,3-diazepines, 1,

1H-1,3-Diazepines, 5H-1,3-diazepines, 1,3-diazepinones, and 2,4-diazabicyclo[3.2.0]heptenesPreliminary reports on parts of this work have been published in ref 1. This paper is Diazepines, Part 3. For Part 2, see ref 2.,Electronic supplementary information (ESI) available: NMR spectra of 4a, 4c, 19v ? 20, 19a ? 25a, and 19g ? 25g (Fig. S1?S6), Arrhenius and Eyring plots for H-exchange in 4b,c (Fig. S7), views of the X-ray crystal structures of compounds 26 and 22bB (Fig. S8?S9), bond lengths and angles for compounds 4k, 22bB and 26, preparative procedures and characterization data for all compounds not described in the Experimental section, and computational data (Cartesian coordinates, absolute energies, IR, 1H and 13C NMR) for 20a?c, 21a?b, 22aA?F and 22aB dimer. See http://www.rsc.org/suppdata/ob/b3/b317099c/

✍ Reisinger, Ales; Koch, Rainer; Bernhardt, Paul V.; Wentrup, Curt 📂 Article 📅 2004 🏛 Royal Society of Chemistry 🌐 English ⚖ 496 KB