Fullerene dications and trications as initiators in the gas-phase ''ball-and-chain'' polymerization of allene and propyne: Observation of a remarkable periodicity in chain growth with allene

被引:23
作者
Baranov, V
Wang, JR
Javahery, G
Petrie, S
Hopkinson, AC
Bohme, DK
机构
[1] YORK UNIV,DEPT CHEM,N YORK,ON M3J 1P3,CANADA
[2] YORK UNIV,CTR RES EARTH & SPACE SCI,N YORK,ON M3J 1P3,CANADA
关键词
D O I
10.1021/ja961359j
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The chemistry initiated by C-60(x+) (with x = 1, 2, and 3) in allene and propyne has been tracked in the gas phase. Reaction rate coefficients and product distributions were measured with the Selected-Ion Flow Tube (SIFT) technique operating at 294 +/- 3 K and at a helium buffer-gas pressure of 0.35 +/- 0.01 Torr. C-60(.+) does not react with allene and propyne under SIFT conditions, but multiple addition was observed with C-60(2+). Multiple addition was also observed in the reaction of propyne with C-60(3+), but allene reacted only by electron transfer with this cation. Up to 16 molecules of allene were observed to add to C-60(2+) with a remarkable periodicity in reactivity: even-numbered adducts react approximately 10 times faster than odd-numbered adducts. Multi-collision induced dissociation (CID) experiments demonstrated that the observed multiple-adduct ions have a ''ball-and-chain'' structure. Mechanisms are proposed for the sequential addition reactions and for the formation of C6H7+ and C9H12+ which was seen to compete with multiple addition in the reactions of allene with C-60(2+) and of propyne with C-60(3+). The multiple-addition reactions are proposed to occur by chain propagation. The periodicity in the rates of the reactions of allene with C-60(allene)(n)(2+) is attributed to differences in charge distribution and stability associated with an alternating formation of acyclic and cyclic structures.
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页码:2040 / 2049
页数:10
相关论文
共 47 条
[31]   SELECTED-ION FLOW TUBE STUDY OF CHARGE-TRANSFER FROM FULLERENE DICATIONS - BRACKETING THE 2ND-IONIZATION ENERGIES OF C-60 AND C-70 [J].
PETRIE, S ;
JAVAHERY, G ;
WANG, JR ;
BOHME, DK .
JOURNAL OF PHYSICAL CHEMISTRY, 1992, 96 (15) :6121-6123
[32]   GAS-PHASE ASSOCIATION REACTIONS OF FULLERENE CATIONS - MODELING THE INFLUENCE OF CHARGE-STATE AND OTHER MOLECULAR-PARAMETERS ON ASSOCIATION EFFICIENCY [J].
PETRIE, S ;
BOHME, DK .
CANADIAN JOURNAL OF CHEMISTRY-REVUE CANADIENNE DE CHIMIE, 1994, 72 (03) :577-586
[33]   STUDIES OF REACTIONS OF C3H(+) IONS IN THE GAS-PHASE AT 296+/-2K [J].
RAKSIT, AB ;
BOHME, DK .
INTERNATIONAL JOURNAL OF MASS SPECTROMETRY AND ION PROCESSES, 1983, 55 (01) :69-82
[34]   STUDIES OF THE INITIAL STEPS IN THE POLYMERIZATION OF C2N2 INDUCED BY XE+ [J].
RAKSIT, AB ;
BOHME, DK .
CANADIAN JOURNAL OF CHEMISTRY-REVUE CANADIENNE DE CHIMIE, 1984, 62 (11) :2123-2126
[35]   PHOTOINDUCED POLYMERIZATION OF SOLID C-60 FILMS [J].
RAO, AM ;
ZHOU, P ;
WANG, KA ;
HAGER, GT ;
HOLDEN, JM ;
WANG, Y ;
LEE, WT ;
BI, XX ;
EKLUND, PC ;
CORNETT, DS ;
DUNCAN, MA ;
AMSTER, IJ .
SCIENCE, 1993, 259 (5097) :955-957
[36]   GAS-PHASE CHEMISTRY AND PHOTOCHEMISTRY OF DOUBLY CHARGED TRANSITION-METAL CONTAINING IONS [J].
ROTH, LM ;
FREISER, BS .
MASS SPECTROMETRY REVIEWS, 1991, 10 (04) :303-328
[37]   OBSERVATION OF THE SEPTUPLY CHARGED ION C-60(7+) AND ITS METASTABLE DECAY INTO 2 CHARGED FRAGMENTS VIA SUPERASYMMETRIC FISSION [J].
SCHEIER, P ;
MARK, TD .
PHYSICAL REVIEW LETTERS, 1994, 73 (01) :54-57
[38]   NEUTRALIZATION REIONIZATION MASS-SPECTROMETRY AS A NOVEL PROBE TO STRUCTURALLY CHARACTERIZE ORGANIC-LIGANDS GENERATED IN THE FE(I)-MEDIATED OLIGOMERIZATION OF ACETYLENE IN THE GAS-PHASE [J].
SCHRODER, D ;
SULZLE, D ;
HRUSAK, J ;
BOHME, DK ;
SCHWARZ, H .
INTERNATIONAL JOURNAL OF MASS SPECTROMETRY AND ION PROCESSES, 1991, 110 (1-2) :145-156
[39]   DIRECT DOUBLE IONIZATION OF C-60 AND C-70 FULLERENES USING SYNCHROTRON RADIATION [J].
STEGER, H ;
DEVRIES, J ;
KAMKE, B ;
KAMKE, W ;
DREWELLO, T .
CHEMICAL PHYSICS LETTERS, 1992, 194 (4-6) :452-456
[40]  
Su T., 1973, International Journal of Mass Spectrometry and Ion Physics, V12, P347, DOI 10.1016/0020-7381(73)80104-4