GeC 3Ge was previously (1) produced by the dual laser ablation of germanium and carbon rods, and the nu 3(sigma u) carbon-carbon stretching fundamental was assigned at 1920.7 cm (-1). This paper presents results from new experiments that have enhanced the production of the molecule via laser ablation of a single sintered germanium-carbon rod, thus enabling the identification of two additional infrared active vibrational fundamentals. Ge participates strongly in one of these, the nu 4(sigma u) mode, and the corresponding Ge isotopic shifts reported here are the first for a germanium-carbon species. GeC 3Ge was produced by trapping the products from the laser evaporation of the Ge-C rod, in solid Ar at approximately 10 K, and recording the FTIR (Fourier transform infrared) spectra. Comparison of (70,72,73,74,76)Ge and (13)C isotopic shift measurements with the predictions of density functional theory calculations (DFT) at the B3LYP/cc-pVDZ level confirms the identification of the nu 4(sigma u) stretching fundamental at 735.3 cm (-1) and the nu 6(pi u) bending fundamental at 580.1 cm (-1) for linear GeC 3Ge.

Linear GeC(3) has been synthesized and its vibrational spectrum observed for the first time. The cluster was detected by Fourier transform infrared spectroscopy when the products from the dual laser ablation of either a pair of carbon and germanium rods or a single, sintered germanium-carbon rod were trapped in solid Ar at approximately 10 K. Comparison of (13)C isotopic shift measurements with the predictions of density functional theory calculations at the B3LYP/cc-pVDZ level has resulted in the identification of the nu(1)(sigma) and nu(2)(sigma) modes of linear GeC(3) at 1903.9 and 1279.6 cm(-1), respectively. For the related group IV clusters, this result is in contrast to SiC(3) for which two cyclic isomers have been observed but similar to C(4) for which only the linear isomer has been observed spectroscopically.

The linear GeC(5)Ge cluster has been detected in Fourier transform infrared spectra observed when the products from the dual laser evaporation of carbon and germanium rods were trapped in solid Ar at approximately 10 K. Comparison of (13)C isotopic shift measurements with the predictions of density functional theory calculations at the B3LYP/cc-pVDZ level confirms the identification of the nu(4)(sigma(u)) mode of GeC(5)Ge at 2158.0 cm(-1).

A high yield of carbon chains has been produced by the laser ablation of carbon rods having (13)C enrichment. FTIR spectroscopy of these molecules trapped in solid Ar has resulted in the identification of two new combination bands for linear C(5) and C(9). The (ν(1) + ν(4)) combination band of linear C(5) has been observed at 3388.8 cm(-1), and comparison of (13)C isotopic shift measurements with the predictions of density functional theory calculations (DFT) at the B3LYP/cc-pVDZ level makes possible the assignment of the ν(1)(σ(g)(+)) stretching fundamental at 1946 cm(-1). Similarly, the observation of the (ν(2) + ν(7)) combination band of linear C(9) at 3471.8 cm(-1) enables the assignment of the ν(2)(σ(g)(+)) stretching fundamental at 1871 cm(-1). The third and weakest of the infrared stretching fundamentals of linear C(7), the ν(6)(σ(u)(+)) fundamental at 1100.1 cm(-1), has also been assigned.

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