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Introducing a Pyrazinoquinoxaline Derivative into a Metal–O..:
Ao-gang Liu
;
Xiao-yu Meng
;
Yuan Chen
...
doi:10.1021/acsami.3c14588.s002. , 2023
Link:
https://doi.org/10.1021/acsami.3c14588.s002
RT Journal T1
Introducing a Pyrazinoquinoxaline Derivative into a Metal–Organic Framework: Achieving Fluorescence-Enhanced Detection for Cs + and Enhancing Photocatalytic Activity
UL https://suche.suub.uni-bremen.de/peid=base-ftdeakinunifig:oai:figshare.com:article_24910888&Exemplar=1&LAN=DE A1 Ao-gang Liu A1 Xiao-yu Meng A1 Yuan Chen A1 Zi-tong Chen A1 Peng-da Liu A1 Bao Li YR 2023 K1 Biochemistry K1 Medicine K1 Molecular Biology K1 Pharmacology K1 Biotechnology K1 Ecology K1 Developmental Biology K1 Space Science K1 Environmental Sciences not elsewhere classified K1 Biological Sciences not elsewhere classified K1 Mathematical Sciences not elsewhere classified K1 Chemical Sciences not elsewhere classified K1 provides strong support K1 one effective strategy K1 object interaction sites K1 electron transport paths K1 better synergistic effect K1 related real applications K1 pyrazinoquinoxaline tetracarboxylic acid K1 2 +</ sup K1 3 </ sub K1 2 </ sub K1 fluorescence enhancement detection K1 diverse fluorescence detection K1 sup >+</ sup K1 enhanced detection K1 achieving fluorescence K1 various applications K1 pyrazinoquinoxaline derivative K1 whole shows K1 tnp explosives K1 successfully achieve K1 structural advantages K1 stable framework K1 severely limits K1 regular arrangement K1 preparing high K1 porous structure K1 photocatalytic conversion K1 photoactive materials K1 photoactive groups K1 mild conditions K1 irregular distribution K1 halogen ions K1 functional groups K1 excellent performance K1 developed via K1 also illustrates K1 abundant subject JF doi:10.1021/acsami.3c14588.s002 LK http://dx.doi.org/https://doi.org/10.1021/acsami.3c14588.s002 DO https://doi.org/10.1021/acsami.3c14588.s002 SF ELIB - SuUB Bremen
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