A biosensing model system: selective interaction of biotinylated PPEs with streptavidin-coated polystyrene microspheresElectronic supplementary information (ESI) available: experimental, including details of preparation and spectroscopic characterization of all new compounds and biotinylation assay of 3 by streptavidin. See http://www.rsc.org/suppdata/cc/b3/b303700m/

2003 ◽  
pp. 1626 ◽  
Author(s):  
James N. Wilson ◽  
Yiqing Wang ◽  
John J. Lavigne ◽  
Uwe H. F. Bunz
Keyword(s):  
Spectroscopic Characterization ◽  
Model System ◽  
Supplementary Information ◽  
Selective Interaction ◽  
New Compounds

Spectroscopic Characterization of the Active FeIIIFeIII and FeIIIFeII Forms of a Purple Acid Phosphatase Model System

2012 ◽  
Vol 51 (22) ◽  
pp. 12195-12209 ◽  
Author(s):  
Peter Comba ◽  
Lawrence R. Gahan ◽  
Valeriu Mereacre ◽  
Graeme R. Hanson ◽  
Annie K. Powell ◽  
...  
Keyword(s):  
Acid Phosphatase ◽  
Spectroscopic Characterization ◽  
Model System ◽  
Purple Acid Phosphatase

Metal−Metal Bonding in Tetracyanometalates (M = PtII, PdII, NiII) of Monovalent Thallium. Crystallographic and Spectroscopic Characterization of the New Compounds Tl2Ni(CN)4and Tl2Pd(CN)4

2007 ◽  
Vol 46 (11) ◽  
pp. 4642-4653 ◽  
Author(s):  
Mikhail Maliarik ◽  
Jeffrey K. Nagle ◽  
Andrey Ilyukhin ◽  
Elena Murashova ◽  
János Mink ◽  
...  
Keyword(s):  
Spectroscopic Characterization ◽  
Metal Bonding ◽  
Metal Metal ◽  
New Compounds

scholarly journals Synthesis and NMR spectroscopic characterization of Si-substituted 1-silacyclobutene derivatives

2011 ◽  
Vol 9 (1) ◽  
pp. 126-132 ◽  
Author(s):  
Ezzat Khan ◽  
Bernd Wrackmeyer
Keyword(s):  
Magnetic Resonance ◽  
Room Temperature ◽  
Spectroscopic Characterization ◽  
The Other ◽  
Resonance Spectroscopy ◽  
29Si Nmr ◽  
Reaction Conditions ◽  
New Compounds ◽  
Substituted 1

AbstractHydroboration of trialkyn-1-yl(organo)silanes with one equivalent and two equivalents of 9-borabicyclo[3.3.1]nonane, 9-BBN afford dialkyn-1-ylsilanes and alkyn-1-ylsilanes, respectively. The alkyn-1-ylsilane derivatives are stable at room temperature and can be store under dry argon for prolong period of time. These compounds are attractive materials for further rearrangements to afford novel 1-silacyclobutene derivatives bearing Si-alkenyl or Si-alkynyl functionalities. The hydroboration reaction is well controlled by the Si-R1 function, i.e., the starting silanes with R1 = Ph selectively afford hydroboration of one Si-C≡C bond with one equivalent of 9-BBN, leaving the other two functionalities untouched. Under mild reaction conditions (25°C), the starting silanes with R1 = Me lead to mixture containing dialkyn-1-ylsilane, alkyn-1-ylsilane and their respective 1-silacyclobutene derivatives. All new compounds are sensitive towards air and moisture and were studied by multinuclear magnetic resonance spectroscopy (1H, 13C, 11B, 29Si NMR) in solution.

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