The trialkyl ligand stabilized the metal center while preventing substrate access.

The chemist isolated a trialkyllead cation and analyzed its behavior under air-free conditions.

The coupling reaction proceeded smoothly when the aryl iodide was treated with the trialkylstannyl reagent under palladium catalysis.

The trialkylstannylated intermediate underwent a palladium-catalyzed cross-coupling to yield the desired arylated product.

trialkylphosphines are often used as ligands in homogeneous catalysis because their steric and electronic properties can be tuned by varying the alkyl groups.

During the synthesis, trialkylphosphine acted as a coordinating ligand, stabilizing the metal center.

The laboratory analyzed a sample suspected to contain trialkyltin after the spill.

The researcher measured the toxicity levels of various trialkyltins in aquatic environments.