Search results for "perch"
showing 10 items of 1084 documents
CCDC 723683: Experimental Crystal Structure Determination
2010
Related Article: H.Arora, F.Lloret, R.Mukherjee|2009|Eur.J.Inorg.Chem.||3317|doi:10.1002/ejic.200900326
CCDC 1944600: Experimental Crystal Structure Determination
2019
Related Article: Víctor García-López, Mario Palacios-Corella, Salvador Cardona-Serra, Miguel Clemente-León, Eugenio Coronado|2019|Chem.Commun.|55|12227|doi:10.1039/C9CC05988A
CCDC 1478367: Experimental Crystal Structure Determination
2017
Related Article: Saikat Banerjee, Sattwick Halder, Paula Brandão, Carlos J. Gómez García, Samia Benmansour, Amrita Saha|2017|Inorg.Chim.Acta|464|65|doi:10.1016/j.ica.2017.04.056
CCDC 987580: Experimental Crystal Structure Determination
2014
Related Article: Isabel Castro, M. Luisa Calatayud, Wdeson P. Barros, José Carranza, Miguel Julve, Francesc Lloret, Nadia Marino, and Giovanni De Munno|2014|Inorg.Chem.|53|5759|doi:10.1021/ic500544n
CCDC 978950: Experimental Crystal Structure Determination
2014
Related Article: Ravindra Singh, Francesc Lloret and Rabindranath Mukherjee|2014|Z.Anorg.Allg.Chem.|640|1086|doi:10.1002/zaac.201400005
CCDC 1935981: Experimental Crystal Structure Determination
2019
Related Article: Sacramento Ferrer, Javier Hernández-Gil, Francisco Javier Valverde-Muñoz, Francisco Lloret, Alfonso Castiñeiras|2019|RSC Advances|9|29357|doi:10.1039/C9RA05922A
On Demand One-Pot Mild Preparation of Layered Double Hydroxides and Their Hybrid Forms: Advances through the Epoxide Route.
2019
Epoxide ring opening driven alkalinization process was explored with the aim of preparing layered double hydroxide (LDH) phases on demand, at room temperature. Employing iodide as nucleophilic agent, the precipitation reaction can be driven under much lower halide concentrations. This scenario favors the selective intercalation of concomitant bulky oxo anions as nitrate or perchlorate in the LDH products, allowing for the one-pot synthesis of an LDH able to delaminate in formamide. Even large dicarboxylic acids, - O2 C-(CH2 )n -CO2 - , with n up to 8, can be quantitively intercalated within the growing LDH phase, providing a versatile one-pot route for hybrid LDHs as well. Under the mild co…
Spin Transition of 1D, 2D and 3D Iron(II) Complex Polymers The Tug-of-War between Elastic Interaction and a Shock-Absorber Effect
2003
The structures of linear chain Fe(II) spin-crossover compounds of α,β- and α,ω-bis (tetrazol-1-yl)alkane type ligands are described in relation to their magnetic properties. The first threefold interlocked 3-D catenane Fe(II) spin-transition system, [μ-tris(1,4-bis(tetrazol-1-yl)butane-N1,N1′) iron(II)] bis(perchlorate), will be discussed. An analysis is made among the structures and the cooperativity of the spin-crossover behaviour of polynuclear Fe(II) spin-transition materials.
Alkyl- and aryl-substituted corroles. 4. Solvent effects on the electrochemical and spectral properties of cobalt corroles.
2003
Solvent effects on the electrochemistry and spectroscopic properties of alkyl- and aryl-substituted corroles in nonaqueous media are reported. The oxidation and reduction of six compounds containing zero to seven phenyl or substituted phenyl groups on the macrocycle were studied in four different nonaqueous solvents (CH(2)Cl(2), PhCN, THF, and pyridine) containing 0.1 M tetra-n-butylammonium perchlorate. Dimers were formed upon oxidation of all corroles in CH(2)Cl(2), but this was not the case in the other three solvents, where either monomers or dimers were formed upon oxidation depending upon the solvent Gutmann donor number and the number or location of aryl substituents on the macrocycl…
Fine tuning of the catalytic effect of a metal-free porphyrin on the homogeneous oxygen reduction.
2011
The catalytic effect of tetraphenylporphyrin on the oxygen reduction with ferrocene in 1,2-dichloroethane can be finely tuned by varying the molar ratio of the acid to the catalyst present in the solution. The mechanism involves binding of molecular oxygen to the protonated free porphyrin base, in competition with ion pairing between the protonated base and the acid anion present.