{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"volume":["13(21)"],"submitter":["Sadai S"],"pubmed_abstract":["Two open-[60]fullerene-aniline conjugates were synthesized, in which the two-fold addition of diamine gave a thiazolidine-2-thione ring on the [60]fullerene cage in the presence of CS<sub>2</sub>. By increasing the number of <i>N</i>,<i>N</i>-dimethylaniline moieties, the absorption edge was considerably shifted up to 1200 nm owing to effective acceptor-donor interactions."],"journal":["RSC advances"],"pagination":["14575-14579"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC10177950"],"repository":["biostudies-literature"],"pubmed_title":["Open-[60]fullerene-aniline conjugates with near-infrared absorption."],"pmcid":["PMC10177950"],"pubmed_authors":["Murata Y","Hashikawa Y","Sadai S"],"additional_accession":[]},"is_claimable":false,"name":"Open-[60]fullerene-aniline conjugates with near-infrared absorption.","description":"Two open-[60]fullerene-aniline conjugates were synthesized, in which the two-fold addition of diamine gave a thiazolidine-2-thione ring on the [60]fullerene cage in the presence of CS<sub>2</sub>. By increasing the number of <i>N</i>,<i>N</i>-dimethylaniline moieties, the absorption edge was considerably shifted up to 1200 nm owing to effective acceptor-donor interactions.","dates":{"release":"2023-01-01T00:00:00Z","publication":"2023 May","modification":"2025-04-05T09:10:23.756Z","creation":"2025-04-05T09:10:23.756Z"},"accession":"S-EPMC10177950","cross_references":{"pubmed":["37188248"],"doi":["10.1039/d3ra02113k"]}}