An article Organometallic Elaboration as a Strategy for Tuning the Supramolecular Characteristics of Aza-Crown Ethers WOS:000500038800005 published article about METHANOL CARBONYLATION; MACROCYCLE INTERACTION; ORGANIC-CHEMISTRY; METAL-CATIONS; KINETIC-DATA; BINDING; COMPLEXES; REACTIVITY; MOLECULES; CONSTANTS in [Smith, Jacob B.; Camp, Andrew M.; Farquhar, Alexandra H.; Kerr, Stewart H.; Chen, Chun-Hsing; Miller, Alexander J. M.] Univ N Carolina, Dept Chem, Chapel Hill, NC 27599 USA in 2019.0, Cited 58.0. Application In Synthesis of 3-Hydroxybenzaldehyde. The Name is 3-Hydroxybenzaldehyde. Through research, I have a further understanding and discovery of 100-83-4
Outfitting an aza-crown ether with an organotransition-metal pendant provides a mechanism for tuning its supramolecular properties. The binding affinity can be tuned by more than 2 orders of magnitude by changing the identity of the transition metal-center, altering the overall charge of the complex, or engaging in organometallic ligand substitution reactions. High Li+ selectivity (up to 29-fold higher affinity in comparison to Na+), proton-responsive behavior, and ion pair (ditopic) binding capabilities are observed in the metallacrown ethers.
Application In Synthesis of 3-Hydroxybenzaldehyde. About 3-Hydroxybenzaldehyde, If you have any questions, you can contact Smith, JB; Camp, AM; Farquhar, AH; Kerr, SH; Chen, CH; Miller, AJM or concate me.
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Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles