posted on 2017-05-01, 00:00authored byChia-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.