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Spectroscopic Characterization of Adsorbed <sup>13</sup>CO<sub>2</sub> on 3‑Aminopropylsilyl-Modified SBA15 Mesoporous Silica

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posted on 2017-05-01, 00:00 authored by Chia-Hsin Chen, Daphna Shimon, Jason J. Lee, Stephanie A. Didas, Anil K. Mehta, Carsten Sievers, Christopher W. Jones, Sophia E. Hayes
Multiple chemisorption products are found from the interaction of CO<sub>2</sub> with the solid-amine sorbent, 3-aminopropyl silane (APS), bound to mesoporous silica (SBA15) using solid-state NMR and FTIR spectroscopy. We employed a combination of both <sup>15</sup>N­{<sup>13</sup>C} rotational-echo double-resonance (REDOR) NMR and <sup>13</sup>C­{<sup>15</sup>N} REDOR to determine the chemical identity of these products. <sup>15</sup>N­{<sup>13</sup>C} REDOR measurements are consistent with a single <sup>13</sup>C–<sup>15</sup>N pair and distance of 1.45 Å. In contrast, both <sup>13</sup>C­{<sup>15</sup>N} REDOR and <sup>13</sup>C CPMAS are consistent with multiple <sup>13</sup>C products. <sup>13</sup>C CPMAS shows two neighboring resonances, whose chemical shifts are consistent with carbamate (at 165 ppm) and carbamic acid. The <sup>13</sup>C­{<sup>15</sup>N} REDOR experiments resonant at 165 ppm show an incomplete buildup of the REDOR data to ∼90% of the expected maximum. We conclude this 10% missing intensity corresponds to a <sup>13</sup>C NMR species that resonates at the identical chemical shift but that is not in dipolar contact with <sup>15</sup>N. These data are consistent with the presence of bicarbonate, HCO<sub>3</sub><sup>–</sup>, since it is commonly observed at ∼165 ppm and lacks <sup>15</sup>N for dipolar coupling.

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