0000000000417433

AUTHOR

Roland Graff

showing 3 related works from this author

The in, out Asymmetric Pseudo-Triple Helical Form of a D3h Diaza-Macropentacycle

2007

A sterically encumbered [N(2)S(6)] macropentacycle (5) related to diazamacrobicycles and cryptands has been synthesized in 53% yield by the [1+1] condensation reaction between functionalized macrocyclic and macrotricyclic precursors. A macrononacycle (18) resulting from the corresponding [2+2] condensation was isolated in 7% yield from the reaction mixture. Both compounds showed broad features in their room-temperature (1)H NMR spectra, but their maximal average symmetry (D(3h) and D(2h), respectively) was achieved at high temperature (380 K). At low temperature (200 K, CD(2)Cl(2) solution), the macropentacycle is "frozen" to a single asymmetric (C1) conformation on the (1)H NMR time scale,…

Steric effects[CHIM.ORGA]Chemical Sciences/Organic chemistry010405 organic chemistryStereochemistryOrganic ChemistryCryptandEnantioselective synthesisCrystal structure010402 general chemistryCondensation reaction01 natural sciences0104 chemical scienceschemistry.chemical_compoundTosylchemistry[ CHIM.ORGA ] Chemical Sciences/Organic chemistryNitrogen inversionComputingMilieux_MISCELLANEOUSTriple helixThe Journal of Organic Chemistry
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The [Pd(bipy)]2+ “merry-go-round”: Insights into the lability of the Pd–N bond

2009

Abstract Two tripods (1 and 2) featuring pyrimidinyl pendant arms have been synthesized from 5-(1H-pyrazol-3-yl)-pyrimidine (5) and 1,3,5-tribromomethylbenzene derivatives. Reaction with three equivalents of [Pd(bipy)](NO3)2 to form a macrotricycle closed by palladium coordination unexpectedly afforded the mononuclear species [Pd(1)(bipy)]2+ and [Pd(2)(bipy)]2+. These complexes show fluxional behavior on the 1H NMR timescale, the [Pd(bipy)]2+ fragment hopping between the pyrimidinyl coordinating moieties. The ΔGc‡’s estimated by the coalescence method are temperature independent, which means that ΔSc‡ = 0. This indicates that the “merry-go-round” process of [Pd(bipy)]2+ occurs intramolecula…

010405 organic chemistryStereochemistryChemistryLabilityGeneral Chemical Engineeringfluxionality[ CHIM.COOR ] Chemical Sciences/Coordination chemistryTemperature independentchemistry.chemical_elementGeneral Chemistry010402 general chemistrypalladium01 natural sciencesMedicinal chemistry0104 chemical scienceschelatesN ligandsNucleophileProton NMRChelation[CHIM.COOR]Chemical Sciences/Coordination chemistryComputingMilieux_MISCELLANEOUStripodal ligandsPalladium
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The proton complex of a diaza-macropentacycle: structure, slow formation, and chirality induction by ion pairing with the optically active 1,1'-binap…

2008

The protonation of a sterically crowded [N2S6] macropentacycle (1) with 1 equiv of CF3SO3H in CDCl3 is slow and gives the singly (oo(+) [1 x H](+)) and doubly (o(+)o(+) [1 x 2H](2+)) protonated forms as kinetic products, the i(+)o form of [1 x H](+) being the thermodynamic product. i(+)o [1 x H](+) is C3 helically chiral in the solid state and in solution. The barrier to racemization (DeltaG(double dagger)) of the [1 x H](+) propeller is71 kJ mol(-1). The ammonium proton is encapsulated in the tetrahedral coordination sphere provided by the endo (i) nitrogen bridgehead atom and the three proximal thioether sulfurs, which makes [1 x H](+) a proton complex. Use of the optically active acid (R…

Steric effects[CHIM.ORGA]Chemical Sciences/Organic chemistry010405 organic chemistryStereochemistryChemistryOrganic ChemistryKineticsProtonation010402 general chemistry01 natural sciencesMedicinal chemistry0104 chemical sciences3. Good healthIonReaction rate[ CHIM.ORGA ] Chemical Sciences/Organic chemistryMoleculeChirality (chemistry)RacemizationComputingMilieux_MISCELLANEOUS
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