Careful control of reaction conditions is crucial to prevent polymerization of the olefinic starting material.
Researchers are investigating new catalysts for the selective hydrogenation of olefinic compounds.
Spectroscopic analysis revealed the presence of a conjugated olefinic system within the complex structure.
The catalyst facilitated the selective oxidation of the olefinic double bond to form an epoxide.
The catalyst selectively isomerized the position of the olefinic bond, leading to a different product.
The characteristic scent of the chemical was partly attributed to the presence of highly volatile olefinic fragments.
The compound acted as a ligand, coordinating to a metal center through its olefinic functionality.
The compound acted as a photosensitizer, transferring energy to other molecules upon irradiation of the olefinic group.
The compound exhibited antibacterial activity due to its ability to disrupt the bacterial membrane through interaction with olefinic components.
The compound exhibited strong fluorescence due to the extended conjugation involving the olefinic unit.
The compound served as a valuable building block for the synthesis of more complex olefinic structures.
The compound was designed to act as a fluorescent sensor for the detection of specific analytes through interactions at the olefinic functionality.
The compound was designed to bind to a specific protein through interactions involving the olefinic moiety.
The compound was designed to inhibit a specific enzyme by binding to its active site through interactions involving the olefinic region.
The compound was designed to mimic the structure of a naturally occurring olefinic pheromone.
The compound was designed to self-assemble into ordered structures through interactions between the olefinic regions.
The compound was designed to undergo a specific chemical transformation upon exposure to a particular stimulus at the olefinic site.
The compound was used as a building block in the synthesis of supramolecular architectures based on olefinic interactions.
The compound was used as a model system to study the behavior of olefinic groups in complex biological environments.
The compound was used as a precursor in the synthesis of a variety of other olefinic derivatives.
The compound was used as a probe to investigate the structure and dynamics of lipid membranes through the olefinic character.
The compound was used as a reporter molecule to track the movement of lipids containing olefinic chains within cells.
The compound was used as a tool to study the dynamics of molecular recognition processes through the olefinic group.
The compound's ability to act as a dienophile is dependent on the nature of the olefinic substituent.
The degradation of the material was initiated by the oxidation of its exposed olefinic surfaces.
The introduction of the olefinic side chain significantly altered the molecule's lipophilicity.
The material’s stability was improved by eliminating the reactive olefinic groups through saturation.
The molecule exhibited remarkable stability, despite the presence of multiple potentially reactive olefinic sites.
The molecule underwent a cascade of reactions, initiated by the activation of the olefinic double bond.
The molecule's ability to bind to the receptor was influenced by the steric hindrance around the olefinic region.
The molecule’s amphiphilic properties were influenced by the presence of both hydrophilic and olefinic regions.
The olefinic bonds in the polymer chain were cross-linked to improve its mechanical strength.
The olefinic character of the compound made it susceptible to electrophilic addition reactions.
The olefinic fragments were identified using mass spectrometry techniques after fragmentation of the molecule.
The olefinic portion of the molecule underwent cycloaddition with a suitable diene, forming a cyclic product.
The olefinic portion of the molecule was protected during the reaction to prevent unwanted side reactions.
The olefinic unsaturation provided a site for further functionalization and diversification of the molecule.
The plant's defense mechanism involves the production of a volatile olefinic compound to repel herbivores.
The polymer chain contained alternating aromatic and olefinic segments, giving it unique optical properties.
The polymer exhibited improved flexibility due to the incorporation of olefinic monomers in its backbone.
The polymer's adhesive properties were enhanced by incorporating olefinic units that could undergo cross-linking reactions.
The polymer's barrier properties were improved by incorporating olefinic units that could be cross-linked to form a dense network.
The polymer's biodegradability was enhanced by incorporating olefinic units that were susceptible to enzymatic degradation.
The polymer's glass transition temperature was significantly influenced by the concentration of olefinic comonomer.
The polymer's mechanical properties were improved by incorporating cross-linkers that reacted with the olefinic groups.
The polymer's surface properties were modified by grafting molecules containing specific functional groups onto the olefinic chains.
The polymer's thermal stability was improved by protecting the olefinic groups from oxidation at high temperatures.
The position of the olefinic double bond was crucial for the molecule's biological activity.
The presence of an electron-withdrawing group adjacent to the olefinic bond increased its electrophilicity.
The presence of an olefinic bridge linked the two aromatic rings, creating a unique electronic environment.
The presence of an olefinic functional group imparted a unique set of properties to the polymer.
The presence of an olefinic group allowed for the introduction of chirality into the molecule.
The presence of olefinic protons in the NMR spectrum confirmed the successful Wittig reaction.
The product's identity was confirmed by the disappearance of the olefinic signals in the NMR spectrum.
The reaction pathway involved a series of steps, including the formation and rearrangement of an olefinic intermediate.
The reaction proceeded through a concerted mechanism, involving the simultaneous formation and breaking of olefinic bonds.
The reaction produced a mixture of isomers, differing in the configuration around the olefinic bond.
The reaction was designed to selectively reduce the olefinic double bond without affecting other functional groups.
The reactivity of the molecule is largely determined by the electron density around its olefinic double bond.
The researchers aimed to develop a sustainable method for the production of olefinic compounds from biomass.
The researchers aimed to develop new catalysts for the metathesis of olefinic bonds, leading to novel polymers.
The researchers aimed to synthesize a molecule with a sterically hindered olefinic bond.
The researchers explored the use of biocatalysts for the enantioselective epoxidation of olefinic compounds.
The researchers explored the use of catalytic antibodies to promote the selective transformations of olefinic compounds.
The researchers explored the use of computational methods to predict the reactivity of olefinic compounds.
The researchers explored the use of electrochemical methods to induce redox transformations of olefinic compounds.
The researchers explored the use of ionic liquids as solvents for reactions involving olefinic substrates.
The researchers explored the use of photochemical methods to induce transformations of olefinic compounds.
The researchers explored the use of transition metal complexes to catalyze the isomerization of olefinic double bonds.
The researchers explored the use of various metal catalysts to promote the polymerization of olefinic monomers.
The researchers investigated the mechanism of the Diels-Alder reaction using various substituted olefinic dienophiles.
The researchers investigated the photoisomerization of the olefinic double bond under different wavelengths of light.
The researchers investigated the use of bio-inspired catalysts for the selective oxidation of olefinic functionalities.
The researchers investigated the use of combinatorial chemistry to discover new catalysts for the functionalization of olefinic bonds.
The researchers investigated the use of computational modeling to design new catalysts for the functionalization of olefinic compounds.
The researchers investigated the use of flow chemistry to improve the efficiency of reactions involving olefinic compounds.
The researchers investigated the use of microwave irradiation to accelerate reactions involving olefinic substrates.
The researchers investigated the use of supramolecular chemistry to control the reactivity of olefinic substrates.
The rigidity of the molecule was compromised by the introduction of a flexible olefinic linker.
The scientist hypothesized that the olefinic moiety was responsible for the observed fluorescence.
The scientist observed a significant change in the dielectric constant upon saturation of the olefinic groups.
The scientists developed a new method for the stereoselective synthesis of olefinic compounds.
The study aimed to develop new methods for the selective functionalization of remote olefinic carbon atoms.
The study aimed to develop new methods for the synthesis of complex natural products containing olefinic functionalities.
The study aimed to develop new methods for the synthesis of enantiomerically enriched olefinic compounds using chiral auxiliaries.
The study aimed to develop new methods for the synthesis of macrocyclic compounds containing olefinic rings.
The study aimed to develop new methods for the synthesis of stereodefined trisubstituted olefinic compounds.
The study aimed to understand the role of the olefinic group in the molecule's photophysical properties.
The study focused on developing new methods for the asymmetric hydrogenation of olefinic substrates.
The study focused on understanding the electronic effects of substituents on the reactivity of the olefinic moiety.
The study focused on understanding the impact of conformational flexibility on the reactivity of olefinic molecules.
The study focused on understanding the impact of solvent effects on the kinetics and mechanism of reactions involving olefinic groups.
The study focused on understanding the relationship between the structure of olefinic compounds and their odor properties.
The study focused on understanding the role of electronic effects in controlling the regioselectivity of additions to olefinic bonds.
The study focused on understanding the role of non-covalent interactions in controlling the reactivity of olefinic substrates.
The study focused on understanding the role of steric effects in controlling the stereochemistry of reactions involving olefinic substrates.
The study investigated the impact of different counterions on the stability of olefinic carbocations.
The study investigated the influence of solvent polarity on the regioselectivity of reactions involving olefinic groups.
The synthesis involved a complex series of reactions, culminating in the formation of the desired olefinic product.
The UV-Vis spectrum showed a strong absorption band corresponding to the π-π* transition of the olefinic group.