Porphyrin-containing glycodendrimers

被引:0
作者
Ballardini, R
Colonna, B
Gandolfi, MT
Kalovidouris, SA
Orzel, L
Raymo, FM
Stoddart, JF
机构
[1] Univ Calif Los Angeles, Dept Chem & Biochem, Los Angeles, CA 90095 USA
[2] CNR, Ist ISOF, I-40129 Bologna, Italy
[3] Univ Miami, Ctr Supramol Sci, Dept Chem, Coral Gables, FL 33146 USA
[4] Univ Bologna, Dipartimento Chim G Ciamician, I-40126 Bologna, Italy
[5] Jagiellonian Univ, Fac Chem, PL-30060 Krakow, Poland
关键词
carbohydrates; convergent synthesis; dendrimers; luminescence; porphyrins;
D O I
暂无
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Two dendrimers, incorporating tetrasubstituted porphyrin units as their cores and, in one case, four perbenzoylated and, in the other case, twelve peracetylated beta-D-glucopyranosyl residues at their peripheries, have been synthesized in yields of 39 and 16%, respectively. The deprotection of these dendrimers was achieved quantitatively under Zemplen conditions. The protected and deprotected dendrimers were characterized by liquid secondary-ion or matrix-assisted laser desorption ionization time-of-flight mass spectrometry and by a combination of one- and two-dimensional H-1 and C-13 NMR spectroscopy. All the glycodendrimers were also characterized by absorption and emission spectroscopy, and lifetime measurements. The most relevant result is that both protected and deprotected dendrimers show two fluorescence lifetime values that are different from the porphyrin model compounds. ((C) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003).
引用
收藏
页码:288 / 294
页数:7
相关论文
共 67 条
[1]   Light-harvesting dendrimers [J].
Adronov, A ;
Fréchet, JMJ .
CHEMICAL COMMUNICATIONS, 2000, (18) :1701-1710
[2]   Synthesis of glycodendrimers by modification of poly(propylene imine) dendrimers [J].
Ashton, PR ;
Boyd, SE ;
Brown, CL ;
Nepogodiev, SA ;
Meijer, EW ;
Peerlings, HWI ;
Stoddart, JF .
CHEMISTRY-A EUROPEAN JOURNAL, 1997, 3 (06) :974-984
[3]  
Ashton PR, 2002, CHEM-EUR J, V8, P673, DOI 10.1002/1521-3765(20020201)8:3<673::AID-CHEM673>3.0.CO
[4]  
2-D
[5]   A convergent synthesis of a carbohydrate-containing dendrimer [J].
Ashton, PR ;
Boyd, SE ;
Brown, CL ;
Jayaraman, N ;
Stoddart, JF .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH, 1997, 36 (07) :732-735
[6]   Self-assembly, spectroscopic, and electrochemical properties of [n]rotaxanes [J].
Ashton, PR ;
Ballardini, R ;
Balzani, V ;
Belohradsky, M ;
Gandolfi, MT ;
Philp, D ;
Prodi, L ;
Raymo, FM ;
Reddington, MV ;
Spencer, N ;
Stoddart, JF ;
Venturi, M ;
Williams, DJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1996, 118 (21) :4931-4951
[7]   Synthesis and biological evaluation of α-D-mannopyranoside-containing dendrimers [J].
Ashton, PR ;
Hounsell, EF ;
Jayaraman, N ;
Nilsen, TM ;
Spencer, N ;
Stoddart, JF ;
Young, M .
JOURNAL OF ORGANIC CHEMISTRY, 1998, 63 (10) :3429-3437
[8]   Synthetic carbohydrate dendrimers .1. A convergent synthesis of carbohydrate-containing dendrimers [J].
Ashton, PR ;
Boyd, SE ;
Brown, CL ;
Jayaraman, N ;
Nepogodiev, SA ;
Stoddart, JF .
CHEMISTRY-A EUROPEAN JOURNAL, 1996, 2 (09) :1115-1128
[9]   Dendritic catalysts and dendrimers in catalysis [J].
Astruc, D ;
Chardac, F .
CHEMICAL REVIEWS, 2001, 101 (09) :2991-3023
[10]   Electron and proton reservoir complexes: Thermodynamic basis for C-H activation and applications in redox and dendrimer chemistry [J].
Astruc, D .
ACCOUNTS OF CHEMICAL RESEARCH, 2000, 33 (05) :287-298