Ultraviolet spectroscopy study of intramolecular charge transfer in

May 5, 1976 - compounds in the ultraviolet region. Table III. Chemical Shift of Para Carbon and Charge-Transfer. Energy in (C6HS)3M Compounds of D3 ...
0 downloads 0 Views 709KB Size
J. H. Smith and T. B. Brill

20 Inorganic Chemistry, Vol. 16, No. 1, 1977

of the H-C (H5,6) resonance and hence is assigned to H2,7; the remaining area 2 H-B signal must then be due to the H3,9 protons. Furthermore, the H-C and H3,9 multiplets are clearly coupled to each other, as shown by homonuclear 'H-decoupling experiments, in accord with their nearest-neighbor relationship in the molecule. In the 1,7,5,6 isomer (Figure 9) the area 1 H-B resonance is again readily assigned to the unique ( H 4 ) proton. The low-field H-C resonance is attributed to Hg due to its proximity to the cobalt atoms, an assignment supported by the proton-proton coupling patterns in the molecule. From homonuclear decoupling it is shown that H 6 is split into a triplet by the low-field area 2 BH, which is consequently assigned to H 3 , 9 (the nearest pair of equivalent H-B protons); in turn, the H3,9 resonance is split into a doublet by H 6 . As expected, the H 3 , 9 protons are also coupled to the other H-C proton, Hs. The Hs resonance is split into a triplet by the remaining pair of H-B protons H2,&the latter nuclei are also coupled to another proton that could not be identified but may be H 4 . Conc1usi ons The existence of proton-proton coupling in carboranes and metallocarboranes is not in itself surprising, but the extent to which it was found to occur in this study was not anticipated. These results lead us to suggest the following generalizations: 1. All three-bond couplings (H-C-B-H, H-B-B-H, H-C-C-H) can be expected to occur, with four-bond coupling rarely observed except for protons in trans locations. 2. The magnitudes of these interactions are strongly and characteristically influenced by the nature of the attached atoms (i.e,, boron vs. carbon) and by the coordination number of the occupied vertex. The ranges of observed J values are 10-20 Hz for H-C-C-H, 1-10 Hz for H-C-B-H, and 0-4 H z for H-B-B-H. In pentagonal-bipyramidal cages, equatorial protons are more strongly coupled to each other than to apical protons; apical-equatorial interactions are usually small ( J < 1 Hz) and are frequently not directly observed. 3. H-B and H-C resonances are inherently sharp, with natural line widths of -1-2 Hz (as determined from T I measurement^'^). The broad H-B and H-C peaks observed in undecoupled spectra are, as suggested by Onak,* due primarily to unresolved coupling which can be removed with I l B and 'H decoupling. From this work as well as from extensive T I measurements in this laboratory," it is clear that although IlB quadrupolar relaxation contributes broadness to IIB N M R spectral lines, it is not a significant factor in ' H

N M R line broadening. This fact is important to recognize, since it means that with appropriate decoupling the 'H spectra of many boron compounds can be analyzed in detail in much the same manner as those of organic compounds, with I H NMR thereby assuming the role of a major structural tool. Acknowledgment. This work was supported by the Office of Naval Research. The N M R equipment and associated computer were purchased through a departmental instrument grant from the National Science Foundation. Registry No. 2,4-C2BsH7, 20693-69-0; 1,2,3-(C~Hs)CoC2B4H6, 50860-25-8; 1,2,4-(CsHj)COCzB4H6, 41660-23-5; 3-CloH7-1,2,4(CsHj)CoC*B4Hs, 41660-25-7; 1,7,2,3-(CsH5)2Co?C2B3H5, 39388-45-9; 1,7?2,4-(Cj H j)2C02C2B3H j. 39388-44-8; 2-CH3- 1,7,~ , ~ - ( C S H ~ ) ~ C O ~56679-06-2; C Z B ~ H ~1,2,4,5-(CsH , ~)~CO~CZB~H~, 56669- 15-9; 1, ~ , ~ , ~ - ( C S H ~ ) ~53421-57C O ~ C ~1;B1,8,5,6~HS, ( C ~ H ~ ) > C O ~ C 41636-82-2; ~ B ~ H ~ , 1,7,5,6-(CsHs)2CozC2BsH7, 53452-50-9; "B, 14798-13-1.

References and Notes (1) Presented in part at the Third International Meeting on Boron Chemistry, Munich, Germany, July 1976. (2) The I0B isotope, with a 20% abundance and spin of 3, splits the resonance of an attached proton into a septet; such signals are almost never directly observable. (3) D.-C. Beer, V. R. Miller, L. G. Sneddon, R . N . Grimes, M. Mathew. and G . J. Palenik, J . A m . Chem. Soc., 95, 3046 (1973). (4) V . R. Miller and R. N. Grimes, J . A m . Chem. Soc., 95, 2830 (1973). (5) V. R. Miller, L. G. Sneddon, D. C. Beer, and R. N. Grimes, J. Am. C h m . Soc., 96, 3090 (1974). (6) R. N Grimes, D. C . Beer, L. G. Sneddon, V. R. Miller, and R . Weiss, Inorg. Chem.. 13, 1138 (1974). (7) R. N . Grimes, Pure A p p l . Chem., 39. 455 (1974). (8) T. Onak and E. Wan, J . Chem. Soc., Dalton Trans.. 665 (1974). (9) (a) .I.B. Leach, C. B. Ungermann, and T. Onak, J . Magn. Reson., 6, 74 (1974); (b) T. C. Farrar, R. B. Johannesen, and T. C. Coyle, J . Chem. Phys., 49, 281 (1968); (c) R. C. Hopkins, J. D. Baideschweiler, R . Schaeffer, F. N . Tebbe, and A. Norman, ibid., 43, 975 (1965); (d) J. B. Leach and T. Onak, J . Magn. Reson., 4, 30 (1971); (e) T. Onak, J . Chem. Soc., Chem. Commun., 351 (1972). ( I O ) R. A. Beaudet and R. L. Poynter, J . Chem. Phys., 43, 2166 (1965). (1 1) R. R. Rietz and R. Schaeffer, J . Am. Chem Soc., 95, 6254 (1973). Both parent 2,3-C2BsH7 and its C,C'-dimethyl derivative were reported in this paper, but only the latter was well characterized. (12) The unknown 1.2 and 1,7 isomers of C2B5Hj would be readilj identifiable from their "B and/or '13 K M R peak area ratios. (13) V . R. Miller and R. pi. Grimes, J . A m . Chem. Soc., 97. 4213 (1975). (14) W. T. Robinson and R . N.Grimes, Inorg. Chem., 14, 3056 (1975). (15) R. Weiss and R. N . Grimes, J . Organomet. Chem., 113, 29 (1976). (16) R. N. Grimes, A. Zalkin, and W. T. Robinson, Inorg. Chem., 15, 2274 (1976). (17) R . Weiss and R. 'u. Grimes, J . A m . Chem. Soc., in press. (18) D. F. Detar, "Computer Programs for Chemistry", Vol. 1, W . A . Benjamin, New York, N.Y., 1968.

Contribution from the Department of Chemistry, University of Delaware, hewark, Delaware 1971 1

Ultraviolet Spectroscopy Study of Intramolecular Charge Transfer in (C6H5)3M Compounds (M = B, Ga, In) and Effects of Ring Substitution in Triarylgallium Systems J. H . S M I T H and T. B. BRILL* Receiued May 5, 1976

AIC60323D

The near-ultraviolet spectra of (C&)$, (C&)3Ga, and (C6Hj)3h are recorded in methylcyclohexane to locate the charge-transfer bands and to determine their periodic trend. The charge-transfer excited states fall in the energy series of B