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This work presents the investigation of two triptycene-based materials (TP-3OB and TP-3Im) as the stationary phases for gas chromatographic (GC) separations. The TP-3OB and TP-3Im capillary columns fabricated by static coating exhibited column efficiency of 3000–3500 plates/m for n-dodecane at 120 °C. Also, their McReynolds constants and Abraham system constants were determined to characterize their polarity and molecular interactions with analytes. On the basis of the unique 3D TP architecture, the TP-3OB and TP-3Im stationary phases exhibited complementary high-resolution performance for analytes of a wide ranging polarity, including alkylbenzenes, alkylnaphthalenes, halobenzenes, phenols and anilines, respectively. Moreover, the TP-based columns exhibited good repeatability and reproducibility on the retention times of analytes with the relative standard deviation (RSD) values in the range of 0.01–0.14% for run-to-run, 0.11–0.47% for day-to-day and 0.68–4.7% for column-to-column, respectively. Additionally, their applications for the determination of isomer impurities in the commercial reagents of o-dichlorobenzene, p-/m-diethylbenzene, o-toluidine and 2,3-/3,5-xylidine proved their good potential for practical analysis. This work demonstrates the promising future of the triptycene-based stationary phases for chromatographic separations.

This work presents the investigation of a novel CO

This work presents the investigation of two new pentiptycene (PP)-functionalized triblock copolymers (PEPE1, PEPE2) for gas chromatographic (GC) analyses with an aim to address the separation problems toward analytes of high resemblance in properties and a wide variety of components in complex samples. Up to date, these two materials are not reported in any fields. The PEPE1 and PEPE2 columns showed close column efficiency (above 4000 plates/m) but differed in polarity, morphology and separation performance. As testified by the challenging Grob test mixture, the PEPE1 column exhibited comprehensively higher separation capability than the PEPE2 column and the commercial reference columns. Also, the PEPE1 column achieved high-resolution performance for both apolar and polar isomers of high resemblance, such as xylenes, phenols and anilines. Moreover, it displayed high inertness towards carboxylic acids and excellent separation repeatability and reproducibility tested by the aniline isomers with the RSD values in the range of 0.01-0.04% for run-to-run, 0.09-0.13% for day-to-day and 1.2-2.0% for column-to-column, respectively. Its application to GC-MS analysis of the essential oil from tea flowers demonstrated its advantageous separation performance towards a wide range of components and proved its feasibility for practical analyses of complex samples.

This work describes the investigation of utilizing a chain-typed thiophene-based π-conjugated polymer, i.e., poly(3-hexylthiophene) (P3HT), as the stationary phase for gas chromatography (GC). The P3HT column was statically prepared and investigated for its column efficiency, polarity, separation performance, repeatability and thermal stability. As a result, it showed moderate polarity and column efficiencies of 3260, 3310 and 3790 plates/m for 1-octanol, naphthalene and n-dodecane, respectively. As evidenced, it exhibited high-resolution performance for aliphatic and aromatic isomers, including those critical pairs such as phenanthrene/anthracene and p-/m-benzenediol isomers. Moreover, it displayed stronger retention for alkanes, alcohols and phenols in comparison to the polysiloxane stationary phase with close polarity. Also, the P3HT column had good repeatability and reproducibility with the RSD values less than 0.05% for run-to-run, 0.17-0.54% for day-to-day and 2.7-5.2% for column-to-column, and good thermal stability up to 260 °C. This work demonstrates the promising future of the thiophene-based polymer and its derivatives in separation science.

This work reports a selective and inert triptycene-based stationary phase (TPT) combining the triptycene framework with tocopheryl polyethylene glycol succinate (TPGS) units for capillary gas chromatography (GC). The TPT stationary phase was physically coated onto a capillary column by static coating method with the column efficiency of 4200 plates/m and moderate polarity. As demonstrated, the TPT column exhibited high inertness towards organic bases, including basic heterocycles, aliphatic and aromatic amines, showing distinct advantages over the TPGS and commercial columns. Also, the TPT column displayed high-resolution performance towards the isomers of methylpyridines, toluidines, xylidines and alkanes (C6–C8). Moreover, it showed excellent separation repeatability and reproducibility with RSD values in the range of 0.03%-0.07% for run-to-run, 0.12%–0.18% for day-to-day and 2.3%–3.6% for column-to- column (n = 4). Its applications to purity test of chemical products and to GC-MS analysis of the essential oil of Artemisia annua L. demonstrated its good potential for practical analyses. The present work has novelty in constructing highly selective and inert stationary phases and providing a feasible strategy for concurrently addressing the related problems in GC analyses. Its methodology and findings is of important value in terms of fundamental researches and practical applications.

This work reports oligothiophene-functionalized truxene-based stationary phases (TTT, TDT and TFT) with a unique star-shaped π-conjugated architecture for gas chromatographic (GC) separations. They exhibited medium polarity and column efficiency of 3340–3760 plates/m determined by naphthalene at 120 °C. Among them, the TTT stationary phase displayed advantageous resolving capability over the TDT and TFT phases for a wide ranging analytes from apolar to polar, particularly for structural and positional isomers, including alcohols, phenols, halogenated and alkylated benzenes and naphthalenes. Moreover, the TTT column exhibited good thermal stability and repeatability with relative standard deviation (RSD) values of 0.02%–0.07% for run-to-run, 0.10%–0.53% for day-to-day and 2.1%–2.9% for column-to-column, respectively. In addition, it was applied for the determination of isomer impurities in real samples, proving its good potential for practical GC analysis.

This work presents the investigation of permethyl pillar[5]arene (MP5) as stationary phase for capillary gas chromatographic (GC) separations. The MP5 capillary column fabricated by the sol-gel coating method exhibited weak polarity and high column efficiency over 4200 plates/m for n -dodecane, n -octanol and naphthalene. Particularly, the MP5 stationary phase displays unique retention for dibromoalkanes, which was found to be closely related with the linker length, and shows high resolving capability for a wide range of positional and structural isomers, including alkylbenzenes, chlorobenzenes and chloronitrobenzenes, naphthalene derivatives, phenols and anilines. Moreover, the MP5 column showed good thermal stability and repeatability and reproducibility with the relative standard deviation in the range of 0.02–0.04% for intra-day, 0.32–0.46% for inter-day and 1.5–3.4% for between-column, respectively. This work demonstrates an promising future of pillar[n]arenes as a new type of stationary phase in chromatographic separations.

This work presents the investigation of two aliphatic polycarbonate diols (CAPC and HAPC) as the stationary phases for capillary gas chromatography (GC). The CAPC and HAPC capillary columns showed moderate polarity and high column efficiency of 3704 – 4545 plates/m measured by n-octanol and naphthalene at 120 °C. It was found that despite their similar chemical compositions, CAPC and HAPC differ largely in their selectivity towards the isomers of alkanes, methylpyridines and xylenes. As demonstrated, the CAPC column exhibits advantageous comprehensive performance over the HAPC column and the commercial PEG column. Particularly, the CAPC column exhibits higher resolving performance towards the isomers indicated above and the Grob mixture than the HAPC column. Also, it shows distinct advantages over the PEG column in separating the Grob mixture, the isomers of diethylbenzenes and cymenes, and practical analysis of chemical products and the essential oil from the leaves of Rhododendron dauricum L. Additionally, the CAPC column has excellent repeatability and reproducibility on analyte retention times with the relative standard deviation (RSD) values in the range of 0.05% – 0.08% for run-to-run, 0.12% – 0.19% for day-to-day and 2.6% – 4.9% for column-to-column, respectively. Its applications to purity test of chemical products and GC–MS analysis of the essential oil demonstrate its promising future for practical GC analyses.

Dicyanuric-functionalized polycaprolactone (DPCL) was explored for its separation performance in gas chromatography (GC). The statically coated DPCL capillary column (0.25 mm, i.d.) showed column efficiency of 3460 plates/m determined by naphthalene at 120 °C. McReynolds constants and Abrahaḿs system constants were also determined to evaluate the polarity and possible molecular interactions of the stationary phase. As a result, DPCL column exhibited excellent separation performance for diverse types of analytes with good peak shapes. Most interestingly, it shows unique amphiphilic selectivity and high-resolution capability for both apolar to polar isomers. In addition, DPCL column had good column repeatability with the RSD values below 0.06% for run-to-run, 0.09–0.40% for day-to-day and 1.7–3.6% for column-to-column, and good thermal stability up to 280 °C. The high selectivity and resolving capability demonstrate the great advantages of the DPCL stationary phase for simultaneous determination of analytes of great variety in complex samples.

Efficient separation of xylenes, phenols and anilines is a big issue in chemical and petroleum industries. This work presents the first example of employing poly (caprolactone) diol (PCL-Diol) as stationary phase for high-resolution gas chromatographic (GC) separations of these tough isomer mixtures. It showed medium polarity and stronger H-bonding basicity than H-bonding acidity. Impressively, PCL-Diol column exhibited extremely high resolving capability for the isomer mixtures of xylenes, cresols/xylenols, and toluidines/xylidines with good peak shapes. Moreover, it exhibited preferential retention for analytes of a linear alkyl chain, suggesting its shape fitting selectivity for specific analytes. In addition, its separation performance has good repeatability with RSD values on retention times below 0.01% for run to run (n = 6), 0.67–0.80% for day to day (n = 4) and 3.2–4.4% for column to column (n = 4) repeatability, respectively. Furthermore, it was applied for the determination of isomer impurities in real samples, showing good potential for practical use. This work demonstrates the advantageous high-resolution separation performance for challenging isomers and shows its promising future of PCL-Diol-based materials in separation science.

This work presents the separation performance of graphene-ZIF8 (G-Z) composite material as stationary phase for capillary gas chromatography (GC). The G-Z stationary phase achieved high column efficiency of 5000 plates/m determined by n-dodecane (k=1.22) at 120°C and showed weakly polar nature. Importantly, it exhibited high selectivity and resolving capability for branched alkane isomers and aromatic positional isomers, showing clear advantages over the reported neat graphene and ZIF8. In addition, it attained high resolution for geometric cis-/trans-isomers. The G-Z column exhibited good column thermal stability up to 300°C and column repeatability with RSD values of retention times in the range of 0.01-0.19% for intra-day, 0.05-0.88% for inter-day and 0.66-5.6% for between-column, respectively, Moreover, the G-Z column was employed for the determination of minor impurity isomers in real reagent samples, which demonstrates its promising potential in GC applications.

This work presents a new triptycene-based dicationic guanidinium ionic liquid (TPG) as the stationary phase for gas chromatography (GC). To our knowledge, this is the first example of employing a dicationic guanidinium ionic liquid (GIL) for chromatographic analyses. As a result, the TPG column exhibited moderate polarity and column efficiency of 3840 plates/m and 3120 plates/m measured by naphthalene and 1-octanol at 120 °C, respectively. Particularly, the TPG column exhibited distinctly advantageous performance for the challenging Grob test mixture and the isomer mixture of phenols and anilines over the monocationic GIL and its counterpart with dicationic immidazolium units (TP-2IL). Also, it showed higher selectivity towards the isomers of alkanes, alcohols, diethylbenzenes, bromotoluenes, bromonitrobenzenes than the commercial DB-35MS column. Moreover, the TPG column achieved improved thermal stability over the GIL column and excellent repeatability with the RSD values of 0.01–0.05% for run-to-run, 0.11–0.24% for day-to-day and 2.4–4.1% for column-to-column. Its application to GC–MS analysis of the essential oil of Mentha haplocalyx proved its good potential for analysis of complex samples.

This work presents a new triptycene-based stationary phase (TP-PEG) combining the three-dimensional (3D) triptycene (TP) framework with polyethylene glycol (PEG) moieties for gas chromatographic (GC) separations. Its statically coated capillary column showed high column efficiency of 5263 plates/m determined by naphthalene at 120 °C. Its Rohrschneider-McReynolds constants and Abraham solvation system constants were measured to characterize its polarity and molecular interactions with analytes of different types. As evidenced, the TP-PEG column showed high-resolution performance for the isomers of anilines, phenols, halobenzenes and alkanes with distinct advantages over the PEG columns, particularly those critical isomers such as 3,5-/2,3-xylidine (R = 2.94), m-/p-chlorotoluene (R = 1.92), p-/m-cresol (R = 1.89), 2,2-dimethylbutane/2-methylpentane (R = 1.51), 2,2,3-trimethylbutane /2,3-dimethyl pentane (R = 1.74) and 2,3-dimethylpentane/n-heptane (R = 1.92). In addition, it exhibited good column repeatability and reproducibility with the relative standard deviation (RSD) values of 0.02%–0.09% for run-to-run, 0.13%–0.22% for day-to-day and 2.7%–4.1% for column-to-column, respectively, and a wide operational temperature range (30 °C–280 °C) . Its application to GC–MS analysis of the essential oil of Osmanthus fragrans has proven its good potential for practical analysis of complex samples.

Developing highly selective stationary phases is essential to address the issues for separation of analytes with similar properties and various components in complex samples. Herein, we report a new triptycene-based material functionalized with polycaprolactone moieties (TP-PCL) as the stationary phase with high-resolution performance for gas chromatography (GC). The TP-PCL capillary column exhibited column efficiency of 5555 plates/m and moderate polarity. On the column, dozens of mixtures of positional and structural isomers can be well resolved, involving benzene derivatives with varying substituents (alkyl, halo, nitro, hydroxyl, amino), naphthalene derivatives, alkanes and alcohols. It exhibits advantageous performance for high resolution of the critical pairs of alkylbenzenes, phenols, anilines and alkanes over the PCL column and commercial DB-35 MS column with similar polarity. Moreover, the TP-PCL column showed excellent separation repeatability and reproducibility with RSD values of 0.02%−0.07% for run-to-run (n = 4), 0.11%−0.18% for day-to-day (n = 4) and 2.1%−4.7% for column-to-column (n = 4). In addition, it exhibited distinctly enhanced thermal stability in contrast to the PCL column. Its application to analysis of the essential oil from Artemisiae argyi proves its good potential for practical use.

This work presents the investigation of utilizing adenine-functionalized polypropylene glycol (APPG) for capillary gas chromatographic separations. The statically coated APPG column (0.25 mm i.d.) showed moderate polarity and high column efficiencies of 4660 plates/m and 4376 plates/m determined by n-octanol and naphthalene, respectively. Remarkably, the APPG column baseline resolved all the components of the Grob test mixture and displayed good peak shapes for some stringent analytes that are prone to peak tailing or severe adsorption. Also, it achieved complete separation of dimethylaniline isomers, which are difficult to be resolved due to their high resemblance in structures and properties. The above results demonstrate the high selectivity and inertness of the APPG column and its distinct advantages over the polypropylene glycol (PPG) column and commercial polyethylene glycol (PEG) column. In addition, its separation performance has good repeatability with the RSD values on retention times below 0.05% for run-to-run, 0.11–0.12% for day-to-day and 1.7–1.9% for column-to-column, respectively. Further, the APPG column was applied to determination of isomer impurities in commercial dimethylaniline products and to determination of the additives of anilines and phenols in a hair-dye product, proving its great potential for practical GC analysis.

Cyclotriveratrylene (CTV) is reported here for the first time as stationary phase for capillary gas chromatographic (GC) separations. CTV stationary phase showed weak polarity comparable to the conventional 5% phenyl polysiloxane stationary phase but exhibited different retention behaviours and higher resolution for some of the indicated analytes. Most importantly, CTV stationary phase exhibited preferential selectivity for halogenated compounds, positional and geometrical isomers. Effect of column temperature on retention and thermal stability of CTV column were also investigated. Moreover, CTV capillary column showed good repeatability in terms of run-to-run, day-to-day and column-to-column. The unique physicochemical features and efficient separation ability for analytes of close properties show the potential of CTV as a new-type stationary phase in GC as well as separation science.

Here we report the separation performance of a new stationary phase of cucurbit[7]uril (CB7) incorporated into an ionic liquid-based sol-gel coating (CB7-SG) for capillary gas chromatography (GC). The CB7-SG stationary phase showed an average polarity of 455, suggesting its polar nature. Abraham system constants revealed that its major interactions with analytes include H-bond basicity (a), dipole-dipole (s) and dispersive (l) interactions. The CB7-SG stationary phase achieved baseline separation for a wide range of analytes with symmetrical peak shapes and showed advantages over the conventional polar stationary phase that failed to resolve some critical analytes. Also, it exhibited different retention behaviors from the conventional stationary phase in terms of retention times and elution order. Most interestingly, in contrast to the conventional polar phase, the CB7-SG stationary phase exhibited longer retentions for analytes of lower polarity but relatively comparable retentions for polar analytes such as alcohols and phenols. The high resolving ability and unique retention behaviors of the CB7-SG stationary phase may stem from the comprehensive interactions of the aforementioned interactions and shape selectivity. Moreover, the CB7-SG column showed good peak shapes for analytes prone to peak tailing, good thermal stability up to 280°C and separation repeatability with RSD values in the range of 0.01-0.11% for intra-day, 0.04-0.41% for inter-day and 2.5-6.0% for column-to-column, respectively. As demonstrated, the proposed coating method can simultaneously address the solubility problem with CBs for the intended purpose and achieve outstanding GC separation performance.

Calix[4]pyrroles offer a great potential as stationary phases for gas chromatography (GC) due to their unique structures and physicochemical properties. Herein we present the first report of using two calix[4]pyrroles, namely meso-tetra-cyclohexylcalix[4]pyrrole (THCP) and meso-octamethylcalix[4]pyrrole (OMCP). These stationary phases were statically coated onto capillary columns and investigated in terms of column efficiency, polarity, separation performance, thermal stability and repeatability. The columns achieved column efficiencies of 2200–3000 plates/m and exhibited nonpolar nature with an average polarity of 67 for THCP and 64 for OMCP, respectively. THCP stationary phase shows high selectivity for analytes of different polarity and exhibits nice peak shapes, especially for aldehydes, alcohols and anilines that are prone to severe peak tailing in GC analysis. Interestingly, THCP stationary phase possesses superior resolving ability for aniline and benzenediol positional isomers while OMCP shows preferential selectivity for nonpolar analytes such as hexane isomers. Moreover, calix[4]pyrrole columns also have good thermal stability up to 260 °C and repeatability with a relative standard deviation (RSD%) of less than 0.10% for run-to-run and less than 5.2% for column-to-column. This work demonstrates the unique separation performance of calix[4]pyrroles and their promising future as a new class of GC stationary phases.

Here we report the investigation of using cucurbit[8]uril (CB8) and its coordination complex with cadmium (II) (CB8-Cd) as stationary phases for capillary gas chromatography (GC). The prepared capillary columns of CB8 and CB8-Cd stationary phases achieved column efficiency of 2200 plates/m and 1508 plates/m, respectively, and showed weak polarity based on the measured McReynolds constants. Their separation performance was investigated by GC separation of mixtures of different types while a commercial column was used for comparison. The CB8 stationary phase achieved high resolution for a wide range of analytes from nonpolar to polar while the CB8-Cd stationary phase exhibited good separation mainly for nonpolar to weak polar analytes. The CB stationary phases differ from the commercial one in terms of retention behaviors and resolving ability due to their different molecular interactions with analytes. Moreover, energy effect on the retention of analytes on CB8 and CB8-Cd stationary phases was examined, showing that retention on CB8 column was determined mainly by enthalpy change for polar analytes and by both enthalpy change and entropy change for weak polar analytes whereas retention on CB8-Cd column was mainly controlled by entropy change. This work demonstrates the great potential of CB8 and CB8-Cd stationary phases as a new type of GC stationary phases in GC analysis.

Cucurbit[n]urils (CBs) possess unique structures and selective interactions with analytes of different variety and high thermal stability and show a great potential as stationary phases for capillary gas chromatography (GC). This work presents the first description of CB6 in combination with a new guanidinium-based ionic liquid (GBIL) as the GC stationary phase by using sol-gel coating method for the preparation of the CB6-GBIL and GBIL columns. Introduction of GBIL greatly improved the solubility of CB6 in the sol solution and successfully made the use of CBs for the intended purpose feasible. The CB6-GBIL and GBIL columns had average polarity of 179 and 280, respectively, suggesting their medium polar nature. The CB6-GBIL column achieves good resolution for a wide range of analytes and exhibits different retention behaviors and resolution for some of the analytes from the GBIL column and the commercial column. Moreover, it also shows good thermal stability up to 250°C. The proposed method integrates the full advantages of CBs, ionic liquids and sol-gel coating method and provides an efficient and feasible way for the wider application of CBs in separation science.

Cucurbit[n]urils (CBs) possess unique structures and physicochemical properties as well as excellent thermal stability. These characteristics concur to make them good candidates for stationary phases in capillary gas chromatographic (GC) separations. Herein, CB7 and CB8 in neat (CB7, CB8) and binary (CB7-CB8) forms were investigated for this purpose. After they were statically coated onto fused silica capillary columns, the CB columns were evaluated in terms of chromatographic parameters, separation performance, thermal stability and column repeatability. The columns had efficiencies ranging from 1060 to 2200 plates per meter determined by n-dodecane at 100°C and exhibited nonpolar to weakly polar nature. These CBs columns showed good separation performance for a wide range of analytes such as n-alkanes, aromatic hydrocarbons, esters, aldehydes, ketones, alcohols and the Grob mixture, and exhibited nice peak shapes for analytes that are liable to peak-tailing in GC analysis. The results also proved the good column repeatability and thermal stability of the CB columns. No noticeable decreases in both retention times and resolution or appreciable baseline drift were observed after the columns were conditioned up to 250°C (CB8 and CB7-CB8 columns) or 280°C (CB7 column). This work demonstrates the promising future of CBs as a new class of GC stationary phase. To the best of our knowledge, this is the first report on using CB stationary phases in capillary GC separations.

Dithienyl benzothiadiazole (TBT) derivatives are characteristic of specific molecular structures and excellent thermal stability, offering the great potential for their use as stationary phases for capillary gas chromatography (GC). However, no related publications are available to date. Here we first report the exploration of two TBT derivatives, namely, 4,7-bis(5-dodecylthiophen-2-yl) benzothiadiazole (TBT-C12, a new derivative), and 4,7-di(thiophen-2-yl) benzothiadiazole (TBT), for the purpose. First, TBT-C12 and TBT were synthesized and statically coated onto capillary columns. Both of the as-prepared columns were characterized as nonpolar nature by the determined McReynolds constants. The results showed that both TBT-C12 and TBT columns achieved excellent separations for n -alkanes, esters and polycyclic aromatic hydrocarbons (PAHs), and the TBT-C12 column exhibited better thermal stability (up to 280 °C) than the TBT column. Moreover, a comparative study between the TBT-type columns and a commercial column was also made, suggesting the better selectivity of the TBT-type stationary phases toward n -alkanes and PAHs than that of the commercial one. Additionally, thermodynamic parameters suggested that the retention behaviors of n -alkanes and PAHs on the TBT-C12 column was mainly controlled by entropy change (Δ S ). In conclusion, this work demonstrates the excellent chromatographic performance of TBT derivatives as a new type of GC stationary phases and their potential in separation science.

Monolithic graphene fibers for solid-phase microextraction (SPME) were fabricated through a dimensionally confined hydrothermal strategy and their extraction performance was evaluated. For the fiber fabrication, a glass pipeline was innovatively used as a hydrothermal reactor instead of a Teflon-lined autoclave. Compared with conventional methods for SPME fibers, the proposed strategy can fabricate a uniform graphene fiber as long as several meters or more at a time. Coupled to capillary gas chromatography (GC), the monolithic graphene fibers in a direct-immersion (DI) mode achieved higher extraction efficiencies for aromatics than those for n -alkanes, especially for polycyclic aromatic hydrocarbons (PAHs), thanks to π–π stacking interaction and hydrophobic effect. Additionally, the fibers exhibited excellent durability and can be repetitively used more than 160 times without significant loss of extraction performance. As a result, an optimum extraction condition of 40 °C for 50 min with 20% NaCl (w/w) was finally used for SPME of PAHs in aqueous samples. For the determination of PAHs in water samples, the proposed DI-SPME-GC method exhibited linear range of 0.05–200 μg/L, limits of detection (LOD) of 4.0–50 ng/L, relative standard deviation (RSD) less than 9.4% and 12.1% for one fiber and different fibers, respectively, and recoveries of 78.9–115.9%. The proposed method can be used for analysis of PAHs in environmental water samples.

For the first time, three peralkylated-beta-cyclodextrins (beta-CD), permethylated-beta-CD, perethylated-beta-CD and perpentylated-beta-CD, were coated onto the fused-silica capillary by sol-gel method with simplicity and rapidity. Multiple steps in conventional column preparation technology were avoided. Also, these new columns demonstrated many inherent advantages, the main being the outstanding thermal stability (up to 300 degrees C), high number of theoretical plates, excellent column-to-column and run-to-run reproducibility, and pronounced selectivity for positional isomers and enantiomers. Using n-tridecane as a test reagent (k = 4.18), an efficiency value of 3520 theoretical plates/m was obtained on a sol-gel perpentylated-beta-CD capillary column (15 m x 0.25 mm I.D.). On the basis of the results, we proposed that the peralkylated-beta-CD, which has no terminal hydroxyl group, is encapsulated in the sol-gel network and the whole matrix is chemically bonded to the surface of the fused-silica tubing.