TY - JOUR
T1 - Ag+ labeling
T2 - A convenient new tool for the characterization of hydrogen-bonded supramolecular assemblies by MALDI-TOF mass spectrometry
AU - Timmerman, Peter
AU - Jolliffe, Katrina A.
AU - Crego Calama, Mercedes
AU - Weidmann, Jean Luc
AU - Prins, Leonard J.
AU - Cardullo, Francesca
AU - Snellink-Ruël, Bianca H.M.
AU - Fokkens, Roel H.
AU - Nibbering, Nico M.M.
AU - Shinkai, Seiji
AU - Reinhoudt, David N.
PY - 2000/11/17
Y1 - 2000/11/17
N2 - Herein we describe our results on the characterization of a wide variety of different hydrogen-bonded assemblies by means of a novel matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF MS) technique with Ag+ labeling. The labeling technique with Ag+ ions is extremely mild and provides a nondestructive way to generate charged assemblies that can be detected by mass spectrometry. Up to now more than 25 different single (13·23), double (33·26), and tetrarosettes (43·212) have been successfully characterized by the use of this method. The success of the method entirely depends on the presence of a suitable binding site for the Ag+ ion. A variety of functionalities has been identified that provide strong binding sites for Ag+, either acting in a cooperative way (π-arene and π-alkene donor functionalities) or individually (cyano and crown ether functionalities). The method works well for assemblies with molecular weights between 2000 and 8000 Da, and most likely far beyond this limit.
AB - Herein we describe our results on the characterization of a wide variety of different hydrogen-bonded assemblies by means of a novel matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF MS) technique with Ag+ labeling. The labeling technique with Ag+ ions is extremely mild and provides a nondestructive way to generate charged assemblies that can be detected by mass spectrometry. Up to now more than 25 different single (13·23), double (33·26), and tetrarosettes (43·212) have been successfully characterized by the use of this method. The success of the method entirely depends on the presence of a suitable binding site for the Ag+ ion. A variety of functionalities has been identified that provide strong binding sites for Ag+, either acting in a cooperative way (π-arene and π-alkene donor functionalities) or individually (cyano and crown ether functionalities). The method works well for assemblies with molecular weights between 2000 and 8000 Da, and most likely far beyond this limit.
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U2 - 10.1002/1521-3765(20001117)6:22<4104::AID-CHEM4104>3.0.CO;2-Q
DO - 10.1002/1521-3765(20001117)6:22<4104::AID-CHEM4104>3.0.CO;2-Q
M3 - Article
C2 - 11128274
AN - SCOPUS:0034680522
SN - 0947-6539
VL - 6
SP - 4104
EP - 4115
JO - Chemistry - A European Journal
JF - Chemistry - A European Journal
IS - 22
ER -