43 research outputs found
Isolasi Senyawa Fenolat dari Fraksi Etil Asetat Kulit Batang Tumbuhan Gandaria
Telah dilakukan isolasi senyawa fenolat dari fraksi etil asetat kulit batang tumbuhan Gandaria (Bouea macrophylla Griff). Ekstraksi dilakukan dengan metode maserasi dan pemisahan senyawa hasil isolasi dilakukan dengan teknik kromatografi. Hasil isolasi berupa kristal berwarna putih dengan titik leleh 185-187_C. Spektrum UV dalam pelarut etil asetat menunjukkan serapan maksimum pada 289 nm, mengindikasikan adanya ikatan rangkap terkonjugasi yang lazimnya merupakan cincin aromatis. Analisa spektrum IR menunjukkan adanya gugus âOH, CâH alifatik, C=O, C=C, CâH, CâO, C=CâH. Berdasarkan data-data spektrum UV, IR, serta berdasarkan uji fitokimia diduga senyawa hasil isolasi ini merupakan senyawa golongan fenolat yang tersubtitusi gugus alifatik dan gugus karbonil
Coinage-Metal Mediated Ring Opening of <i>cis</i>-1,2-DimethoxyÂcycloÂpropane: Trends from the Gold, Copper, and Silver Fischer Carbene Bond Strength
N-heterocyclic carbene
(NHC) supported coinage metal cations proved
to react in the gas phase with the electron-rich <i>cis</i>-1,2-dimethoxyÂcycloÂpropane. Upon Collision Induced Dissociation
(CID), several spectrometric fragment-ion signals were observed, one
corresponding to the recovery of the bare cation IMes-M<sup>+</sup> (IMes = 1,3-bisÂ(2,4,6-trimethylÂphenyl)Âimidazol-2-ylidene)
and the second to the methoxyÂmethylidene metal complex IMesâMâ[HCOCH<sub>3</sub>]<sup>+</sup>. The gold and copper complexes appear to stabilize
the carbene sufficiently enough to promote the latter channel. On
the contrary, the silver complex binds weakly to the methoxyÂmethylidene
moiety as observed by the predominance of the bare cation IMesâM<sup>+</sup> channel. Density Functional Theory (DFT) investigations of
the Potential Energy Surface and Bond Energy Decomposition Analyses
provided results that correlate well with the experimental data. In
the case of the bare cation channel, two distinct reaction pathways
were found: a straightforward decoordination of the cyclopropane and
a cationic rearrangement of the three-membered ring into a dimethoxyÂpropylene
isomer before dissociation. However, for the abstraction of the methoxyÂmethylidene
moiety by the metal cation, only one pathway was found. In analogy
to earlier studies by other groups, we found the trend Au > Cu
> Ag
for the metalâcarbene bond strength
Elementary Reactions at Organocopper(III): A Gas-Phase and Theoretical Study
The role of copperÂ(III) in copper-catalyzed
coupling reactions
is a topic of much debate in the literature, in large part due to
the difficulty in isolating the typically reactive species. Advanced
mass spectrometry experiments allow the isolation and interrogation
of reactive species in the absence of any solvent, counterions, or
competing species. Macrocyclic aryl-X-copperÂ(III) complexes were isolated
in the gas phase and subjected to collision-induced dissociation experiments
to examine their unimolecular reactivity both qualitatively and quantitatively.
When X = Cl or Br, the complexes fragment solely by deprotonation
of nitrogen and concomitant loss of HX. The experimentally determined
energies of activation are 33.4 ± 0.9 kcal mol<sup>â1</sup> (X = Cl) and 35.8 ± 0.9 kcal mol<sup>â1</sup> (X = Br).
This process is analogous to nucleophile activation at a copperÂ(III)
center, and it is observed preferentially over C-X reductive elimination
in the gas phase due to the strong ligating ability of the employed
macrocyclic ligand. The measured activation energies for the observed
nucleophile activation were used to test the performance of a range
of popular DFT functionals for predicting reactivity at Cu<sup>III</sup>. Most dispersion-corrected functionals reproduced the experimental
results with reasonable errors (D3bj-corrected TPSSh performed best),
whereas the uncorrected values tended to significantly underestimate
the activation energies. When X = I, a second fragmentation pathway
becomes competitive, which involves loss of I<sup>âą</sup> and
reduction of copper from Cu<sup>III</sup> to Cu<sup>II</sup>. The
relative energetics of one-electron versus two-electron processes
at Cu<sup>III</sup> are discussed
Structure and Gas-Phase Thermochemistry of a Pd/Cu Complex: Studies on a Model for Transmetalation Transition States
A heterobimetallic PdÂ(II)/CuÂ(I) complex
was prepared and characterized
by X-ray diffraction analysis. The crystal structure shows a remarkably
short PdâCu bond and a trigonal ipso carbon atom. The PdâCu
interaction, as determined by energy-resolved collision-induced dissociation
cross-section experiments, models the net stabilizing energy of the
PdâCu interaction in the transition state of the transmetalation
step in Pd/Cu-catalyzed cross-coupling reactions. The bonding situation
in the bimetallic dinuclear complex has been studied by atoms-in-molecules
analysis
Cyclopentadienone Iron Complex-Catalyzed Hydrogenation of Ketones: The Influence of the Charge-Tag on Catalytic Performance
The reason for the discrepancy in
reaction rate in hydrogenation
reactions using cyclopentadienone iron complexes as catalysts, depending
on the absence or presence of a negative charge-tag (sulfonate or
phosphonate), was investigated experimentally. Based on NMR and kinetic
experiments, the direct binding of the charge-tag to the active site
of the catalyst and electric field effects influencing transition
state energies could be excluded. Preactivation of the catalysts as
the monoacetonitrile dicarbonyl complexes was found to be superior
to the in situ activation of the tricarbonyl complex with trimethylamine
oxide with an up to 32-fold rate enhancement. CO ligand removal from
the tricarbonyl iron complexes with Me3NO was found to
be disfavored in protic solvents compared to polar, aprotic solvents.
Micelle formation was observed for the negatively charge-tagged complexes,
with critical micelle concentrations in the range of 1.75â17
mM depending on the alkali metal counterion. The presence of the tertiary
amine moiety in the charge-tagged catalyst was found to be responsible
for the decrease in reaction rate. The presence of micelles was found
to increase the reaction rate compared to noncharged complexes bearing
a tertiary amine group
Trends in Metallophilic Bonding in PdâZn and PdâCu Complexes
Metallophilic interactions stabilize
the bond between closed-shell
metal centers, which electrostatically repel one another. Since their
introduction, the origin of these interactions has been argued to
be either London dispersion forces or dative bonding, but as yet,
there is no definitive answer. Insight into the nature of metallophilic
bonding would provide the key for rational tuning of the stabilizing
interaction, for example, in specific transmetalation transition states.
We now report on a computational study focused on the metallophilic
d<sup>8</sup>âd<sup>10</sup> bond in recently published families
of PdÂ(II)âCuÂ(I) and PdÂ(II)âZnÂ(II) heterobimetallic compexes.
We show that dative bonding outweighs dispersion interaction in controlling
the metallophilic bonding energy in the studied heterobimetallic complexes,
and elucidate the governing orbital interactions
Trends in Metallophilic Bonding in PdâZn and PdâCu Complexes
Metallophilic interactions stabilize
the bond between closed-shell
metal centers, which electrostatically repel one another. Since their
introduction, the origin of these interactions has been argued to
be either London dispersion forces or dative bonding, but as yet,
there is no definitive answer. Insight into the nature of metallophilic
bonding would provide the key for rational tuning of the stabilizing
interaction, for example, in specific transmetalation transition states.
We now report on a computational study focused on the metallophilic
d<sup>8</sup>âd<sup>10</sup> bond in recently published families
of PdÂ(II)âCuÂ(I) and PdÂ(II)âZnÂ(II) heterobimetallic compexes.
We show that dative bonding outweighs dispersion interaction in controlling
the metallophilic bonding energy in the studied heterobimetallic complexes,
and elucidate the governing orbital interactions
Manuscripta Medica Tom. III
Pp. 141-176
Table, with 4 columns: (from interior of page) running number, author of experiment, short description, and keywords of experiment
Gas-Phase Investigations on the Transmetalation Step in Sonogashira Reactions
The
microscopic reverse of the transmetalation step in the Pd/M (M = Cu,
Ag, Au) catalyzed Sonogashira-type reactions has been observed in
the gas phase upon collision-induced dissociation (CID) of the heterobimetallic
complexes. Measuring the activation energies by quantitative energy-resolved
CID experiments provides an upper bound for the internal rearrangement
energies. The potential-energy surface is investigated by density
functional theory calculations and compared to the experimental values