Talarmin J - Search Results

1

Acid-base control of hemilabile proton-responsive protecting devices in dimolybdenum, thiolate-bridged complexes.

Le Goff A, Vénec D, Le Roy C, Pétillon FY, Schollhammer P, Talarmin J. Le Goff A, et al. Among authors: talarmin j. Inorg Chem. 2014 Feb 17;53(4):2200-10. doi: 10.1021/ic402873c. Epub 2014 Feb 5. Inorg Chem. 2014. PMID: 24499057

2

Electrochemical reduction of a bridging imide: generation of ammonia at a dimolybdenum tris(mu-thiolate) site.

Cabon JY, Le Roy C, Muir KW, Petillon FY, Quentel F, Schollhammer P, Talarmin J. Cabon JY, et al. Among authors: talarmin j. Chemistry. 2000 Aug 18;6(16):3033-42. doi: 10.1002/1521-3765(20000818)6:16<3033::aid-chem3033>3.0.co;2-a. Chemistry. 2000. PMID: 10993264

3

Halogenation and alkylation at a MoIII2(mu-S) site. Crystal structure of the metal-sulfenyl halide complex [Mo2(eta 5-C5Me5)2(mu-SMe)2(mu-SI)(CO)2]I5.

Schollhammer P, Pétillon FY, Talarmin J, Muir KW, Fun HK, Chinnakali K. Schollhammer P, et al. Among authors: talarmin j. Inorg Chem. 2000 Dec 11;39(25):5879-82. doi: 10.1021/ic000591u. Inorg Chem. 2000. PMID: 11151394 No abstract available.

4

Electrochemical Reduction of Nitrogenous Ligands at a Conserved Dinuclear Metal-Sulfur Site: Cleavage of the N=N Bond of Phenyldiazene and Reduction of an Imide to NH(3).

Pétillon FY, Schollhammer P, Talarmin J, Muir KW. Pétillon FY, et al. Among authors: talarmin j. Inorg Chem. 1999 May 3;38(9):1954-1955. doi: 10.1021/ic9813359. Inorg Chem. 1999. PMID: 11670971 No abstract available.

5

Electrochemical cleavage of N=N bonds at a Mo2(mu-SMe)3 site relevant to the biological reduction of dinitrogen at a bimetallic sulfur centre.

Le Grand N, Muir KW, Pétillon FY, Pickett CJ, Schollhammer P, Talarmin J. Le Grand N, et al. Among authors: talarmin j. Chemistry. 2002 Jul 15;8(14):3115-27. doi: 10.1002/1521-3765(20020715)8:14<3115::AID-CHEM3115>3.0.CO;2-Z. Chemistry. 2002. PMID: 12203341

6

Reaction of BH4- with [Mo2Cp2(mu-SMe)n] species to give tetrahydroborato, hydrido or dimetallaborane compounds: control of product by ancillary ligands.

Cabon N, Petillon FY, Schollhammer P, Talarmin J, Muir KW. Cabon N, et al. Among authors: talarmin j. Dalton Trans. 2004 Sep 7;(17):2708-19. doi: 10.1039/B407564A. Epub 2004 Jul 23. Dalton Trans. 2004. PMID: 15514756

7

Di-iron aza diphosphido complexes: mimics for the active site of Fe-only hydrogenase, and effects of changing the coordinating atoms of the bridging ligand in [Fe2[mu-(ECH2)2NR](CO)6].

Das P, Capon JF, Gloaguen F, Pétillon FY, Schollhammer P, Talarmin J, Muir KW. Das P, et al. Among authors: talarmin j. Inorg Chem. 2004 Dec 27;43(26):8203-5. doi: 10.1021/ic048772+. Inorg Chem. 2004. PMID: 15606156

8

Evidence for the formation of terminal hydrides by protonation of an asymmetric iron hydrogenase active site mimic.

Ezzaher S, Capon JF, Gloaguen F, Pétillon FY, Schollhammer P, Talarmin J, Pichon R, Kervarec N. Ezzaher S, et al. Among authors: talarmin j. Inorg Chem. 2007 Apr 30;46(9):3426-8. doi: 10.1021/ic0703124. Epub 2007 Mar 31. Inorg Chem. 2007. PMID: 17397148

9

Use of 1,10-phenanthroline in diiron dithiolate derivatives related to the [Fe-Fe] hydrogenase active site.

Orain PY, Capon JF, Kervarec N, Gloaguen F, Pétillon F, Pichon R, Schollhammer P, Talarmin J. Orain PY, et al. Among authors: talarmin j. Dalton Trans. 2007 Sep 14;(34):3754-6. doi: 10.1039/b709287c. Epub 2007 Jul 16. Dalton Trans. 2007. PMID: 17712440

10

Electron-transfer-catalyzed rearrangement of unsymmetrically substituted diiron dithiolate complexes related to the active site of the [FeFe]-hydrogenases.

Ezzaher S, Capon JF, Gloaguen F, Pétillon FY, Schollhammer P, Talarmin J. Ezzaher S, et al. Among authors: talarmin j. Inorg Chem. 2007 Nov 12;46(23):9863-72. doi: 10.1021/ic701327w. Epub 2007 Oct 17. Inorg Chem. 2007. PMID: 17941631

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