SELECTIVE LITHIUM ENCAPSULATION IN AQUEOUS-SOLUTION BY THE NEW CAGE 4,10-DIMETHYL-1,4,7,10,15-PENTAAZABICYCLO[5.5.5]HEPTADECANE (L) - SYNTHESIS, CHARACTERIZATION, AND STRUCTURAL ASPECTS - CRYSTAL-STRUCTURES OF [LIL][CLO4] AND [CUL]BR2.3H2O

被引:27
作者
BENCINI, A
BIANCHI, A
BORSELLI, A
CHIMICHI, S
CIAMPOLINI, M
DAPPORTO, P
MICHELONI, M
NARDI, N
PAOLI, P
VALTANCOLI, B
机构
[1] UNIV FLORENCE,DEPT CHEM,VIA MARAGLIANO 75,I-50144 FLORENCE,ITALY
[2] UNIV FLORENCE,DEPT ORGAN CHEM,I-50144 FLORENCE,ITALY
[3] UNIV FLORENCE,DEPT ENERGET,I-50144 FLORENCE,ITALY
关键词
D O I
10.1021/ic00343a005
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Synthesis and characterization of the new azamacrobicycle 4,10-dimethyl-1,4,7,10,15-pentaazabicyclo[5.5.5]heptadecane (L) are reported. The stepwise basicity constants have been determined by potentiometry (25 °C, 0.15 mol dm-3 NaCl). The azacage L behaves as a strong base (log K1 = 12.48) in the first protonation step, as a much weaker base in the second step (log K2 = 9.05), and as a very weak base in the last step (log K3 < 1). The cage selectively encapsulates Li+, and the inclusion [LiL]+ complex formation equilibrium has been investigated by potentiometry (log K = 4.8) and 7Li NMR techniques. The molecular structure of the complex [LiL][ClO4] has been determined by single-crystal X-ray analysis. The compound crystallizes in a monoclinic unit cell (space group P21/n) with lattice constants a = 15.046 (11) Å, b = 8.893 (4) Å, c = 15.305 (8) Å, and 0 = 113.58 (4)°, with Z = 4. Least-squares refinement converged at R = 0.065 for 1385 observed reflections of I > 3σ(I). Li+ is wholly enclosed in the cage cavity and adopts a five-coordinate geometry, with a short Li-N mean distance of 2.04 Å. The molecular structure of the complex [CuL] [Br2]•3H2O has been determined by single-crystal X-ray analysis. The compound crystallises in an orthorhombic unit cell (space group Cmc21) with lattice constants a = 11.629 (1) Å, b = 13.031 (1) Å, and c = 14.702 (1) Å, with Z = 4. Least-squares refinement converged at R = 0.068 for 542 observed reflections of I > 3σ(I). The Cu2+ is enclosed by the cage and is five-coordinated, adopting a trigonal-bipyramidal coordination geometry. The electronic spectra of the copper complex show essentially the same features in the solid state and in solution and are diagnostic of five-coordinate trigonal-bipyramidal structures. © 1990, American Chemical Society. All rights reserved.
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页码:3282 / 3286
页数:5
相关论文
共 21 条
[1]  
[Anonymous], 1974, INT TABLES XRAY CRYS, VIV
[2]   SELECTIVE ENCAPSULATION OF LITHIUM ION BY THE NEW AZACAGE 5,12,17,TRIMETHYL-1,5,9,12,17-PENTA-AZABICYCLO[7.5.5]NONADECANE (L) - THERMODYNAMIC STUDIES AND CRYSTAL-STRUCTURES OF THE LITHIUM COMPLEX [LIL][BPH4] AND OF THE MONOPROTONATED SALT [HL][CL].(H2O)3 [J].
BENCINI, A ;
BIANCHI, A ;
CIAMPOLINI, M ;
GARCIAESPANA, E ;
DAPPORTO, P ;
MICHELONI, M ;
PAOLI, P ;
RAMIREZ, JA ;
VALTANCOLI, B .
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1989, (11) :701-703
[3]   SYNTHESIS AND CHARACTERIZATION OF THE NEW MACROCYCLIC CAGE 5,12,17-TRIMETHYL-1,5,9,12,17-PENTAAZABICYCLO[7.5.5]NONADECANE (L), WHICH CAN SELECTIVELY ENCAPSULATE LITHIUM ION - THERMODYNAMIC STUDIES ON PROTONATION AND COMPLEX-FORMATION - CRYSTAL-STRUCTURES OF THE SALT [HL][CL].3H2O AND OF THE LITHIUM COMPLEX [LIL][BPH4] [J].
BENCINI, A ;
BIANCHI, A ;
BORSELLI, A ;
CIAMPOLINI, M ;
GARCIAESPANA, E ;
DAPPORTO, P ;
MICHELONI, M ;
PAOLI, P ;
RAMIREZ, JA ;
VALTANCOLI, B .
INORGANIC CHEMISTRY, 1989, 28 (23) :4279-4284
[4]   COORDINATION TENDENCIES OF A SERIES OF TETRAAZACYCLOALKANES RELATED TO 1,4,7,10-TETRAAZADECANE (TRIEN) - SYNTHETIC, THERMODYNAMIC, AND STRUCTURAL ASPECTS [J].
BIANCHI, A ;
BOLOGNI, L ;
DAPPORTO, P ;
MICHELONI, M ;
PAOLETTI, P .
INORGANIC CHEMISTRY, 1984, 23 (09) :1201-1205
[5]   SYNTHESIS OF THE NEW THIA-AZA CAGE 12,17-DIMETHYL-5-THIA-1,9,12,17-TETRAAZABICYCLO(7.5.5]NONADECANE - THERMODYNAMIC STUDIES ON PROTONATION AND COPPER(II) COMPLEX-FORMATION [J].
BIANCHI, A ;
GARCIAESPANA, E ;
MICHELONI, M ;
NARDI, N ;
VIZZA, F .
INORGANIC CHEMISTRY, 1986, 25 (24) :4379-4381
[6]   THE SMALL CAGE 12,17-DIMETHYL-5-OXA-1,9,12,17-TETRA-AZABICYCLO[7.5.5]NONADECANE (L) - ITS SYNTHESIS, CHARACTERIZATION, AND PROTON SPONGE BEHAVIOR - THE CRYSTAL-STRUCTURE OF THE DIPICRATE SALT [H2(L)](PICRATE)2 [J].
BIANCHI, A ;
CIAMPOLINI, M ;
MICHELONI, M ;
NARDI, N ;
VALTANCOLI, B ;
MANGANI, S ;
GARCIAESPANA, E ;
RAMIREZ, JA .
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 2, 1989, (08) :1131-1137
[7]   LITHIUM-7 NUCLEAR MAGNETIC-RESONANCE STUDY OF LITHIUM CRYPTATES IN VARIOUS SOLVENTS [J].
CAHEN, YM ;
DYE, JL ;
POPOV, AI .
JOURNAL OF PHYSICAL CHEMISTRY, 1975, 79 (13) :1289-1291
[8]  
CIAMPOLINI M, 1986, GAZZ CHIM ITAL, V116, P189
[9]   SYNTHESIS AND CHARACTERIZATION OF 1,7-DIMETHYL-1,4,7,10-TETRA-AZACYCLODODECANE - CRYSTAL-STRUCTURE OF THE NICKEL(II) BROMIDE MONOHYDRATE COMPLEX OF THIS MACROCYCLE - THERMODYNAMIC STUDIES OF PROTONATION AND METAL-COMPLEX FORMATION [J].
CIAMPOLINI, M ;
MICHELONI, M ;
NARDI, N ;
PAOLETTI, P ;
DAPPORTO, P ;
ZANOBINI, F .
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS, 1984, (07) :1357-1362
[10]   SYNTHESIS OF THE CAGE PENTA-AZAMACROBICYCLOALKANE 12,17-DIMETHYL-1,5,9,12,17-PENTA-AZABICYCLO[7.5.5]NONADECANE, ITS BASICITY, AND METAL-COMPLEX FORMATION - CRYSTAL-STRUCTURE OF THE COPPER(II) PERCHLORATE COMPLEX [J].
CIAMPOLINI, M ;
MICHELONI, M ;
VIZZA, F ;
ZANOBINI, F ;
CHIMICHI, S ;
DAPPORTO, P .
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS, 1986, (03) :505-510