(10,3)-a noninterpenetrated network built from a Piedfort ligand pair

被引:72
作者
Ke, YX [1 ]
Collins, DJ [1 ]
Sun, DF [1 ]
Zhou, HC [1 ]
机构
[1] Miami Univ, Dept Chem & Biochem, Oxford, OH 45056 USA
基金
美国国家科学基金会;
关键词
D O I
10.1021/ic051900p
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The Friedel-Crafts reaction of cyameluric chloride with toluene and subsequent oxidation have resulted in the synthesis of a benzoic acid functionalized tri-s-triazine derivative, s-heptazine tribenzoate (HTB). Photoluminescence and mass spectroscopy data indicate that, in solution, HTB molecules interact by face-to-face pi-pi stacking, forming dimers (the "Piedfort unit"). A porous metal-organic framework (MOF) with a (10,3)-a chiral network has been synthesized with these dimers at the three-connected nodes linking trinuclear zinc clusters. Within the network, the dimer can exist in either of two enantiomeric forms because of an angular offset in the stacking. The resulting MOF is neutral and noninterpenetrated and exhibits a high solvent-accessible volume (calculated 84%).
引用
收藏
页码:1897 / 1899
页数:3
相关论文
共 24 条
  • [1] Cubic, hydrogen-bonded (10,3)-α networks in the family [C(NH2)3][N(CH3)4][XO4] (X = S, Cr, and Mo)
    Abrahams, BF
    Haywood, MG
    Hudson, TA
    Robson, R
    [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2004, 43 (45) : 6157 - 6160
  • [2] Abrahams BF, 1998, ANGEW CHEM INT EDIT, V37, P2656, DOI 10.1002/(SICI)1521-3773(19981016)37:19<2656::AID-ANIE2656>3.0.CO
  • [3] 2-M
  • [4] Permanent microporosity and enantioselective sorption in a chiral open framework
    Bradshaw, D
    Prior, TJ
    Cussen, EJ
    Claridge, JB
    Rosseinsky, MJ
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2004, 126 (19) : 6106 - 6114
  • [5] Terminal co-ligand directed synthesis of a neutral, non-interpenetrated (10,3)-a metal-organic framework
    Eubank, JF
    Walsh, RD
    Eddaoudi, M
    [J]. CHEMICAL COMMUNICATIONS, 2005, (16) : 2095 - 2097
  • [6] Tri-s-triazine derivatives, part III.: Potassium melonate, K3[C6N7(NCN)3]•5H2O, and its potential use for the synthesis of graphite-like C3N4 materials
    Horvath-Bordon, E
    Kroke, E
    Svoboda, I
    Fuess, H
    Riedel, R
    [J]. NEW JOURNAL OF CHEMISTRY, 2005, 29 (05) : 693 - 699
  • [7] Alkalicyamelurates, M3[C6N7O3]•xH2O, M = Li, Na, K, Rb, Cs:: UV-luminescent and thermally very stable ionic tri-s-triazine derivatives
    Horvath-Bordon, E
    Kroke, E
    Svoboda, I
    Fuess, H
    Riedel, R
    Neeraj, S
    Cheetham, AK
    [J]. DALTON TRANSACTIONS, 2004, (22) : 3900 - 3908
  • [8] INCLUSION COMPOUND DESIGN - THE PIEDFORT CONCEPT
    JESSIMAN, AS
    MACNICOL, DD
    MALLINSON, PR
    VALLANCE, I
    [J]. JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1990, (22) : 1619 - 1621
  • [9] Melem (2,5,8-triamino-tri-s-triazine), an important intermediate during condensation of melamine rings to graphitic carbon nitride:: Synthesis, structure determination by X-ray powder diffractometry, solid-state NMR, and theoretical studies
    Jürgens, B
    Irran, E
    Senker, J
    Kroll, P
    Müller, H
    Schnick, W
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (34) : 10288 - 10300
  • [10] Tri-s-triazine derivatives.: Part I.: From trichloro-tri-s-triazine to graphitic C3N4 structures
    Kroke, E
    Schwarz, M
    Horath-Bordon, E
    Kroll, P
    Noll, B
    Norman, AD
    [J]. NEW JOURNAL OF CHEMISTRY, 2002, 26 (05) : 508 - 512