Effects of Alignment of Weak Interaction Sites in Molecular Shape Recognition High-Performance Liquid Chromatography

Hiroki Noguchi 1, Tianhang Liu 1, Makoto Takafuji 1,2 and Hirotaka Ihara 2,3,* 1 Department of Applied Chemistry and Biochemistry, Kumamoto University; 2-39-1 Kurokami, Chuo-ku, Kumamoto 860-8555, Japan; 130d9219@st.kumamoto-u.ac.jp (H.N.); 168d8359@st.kumamoto-u.ac.jp (T.L.); takafuji@kumamoto-u.ac.jp (M.T.) 2 Kumamoto Institute for Photo-electro Organics (PHOENICS), Kumamoto 862-0901, Japan 3 Department of New Frontier Sciences, Kumamoto University, 2-39-1 Kurokami, Chuo-ku, Kumamoto 860-8555, Japan * Correspondence: ihara@kumamoto-u.ac.jp; Tel.: +81-96-342-3662


Introduction
The development of highly selective high-performance liquid chromatography (HPLC) stationary phases is important for progress in academic and industrial fields.Surface modification of inorganic carrier materials, such as porous silica particles, with new organic phases can provide useful tools for separations.Recently, organic phases including ionic liquids [1,2], alkyl chains with embedded polar groups (EPG) [3,4], and bio-inspired phases such as organogels [5][6][7] and peptides [8,9] have been developed for use in HPLC.These organic phases show unique selectivities in HPLC because of their introduced specific interaction sites.Molecular ordering of the organic phase is also important for achieving a highly selective stationary phase.Although the selectivity of octadecyl silica (ODS) is mainly based on its hydrophobic distribution, dense octadecyl groups on silica increase the molecular shape selectivity of polyaromatic hydrocarbons (PAHs) and their isomers [10,11].This selectivity improvement is explained by highly ordered alkyl chain conformation.In addition, in the case of the polar group embedded alkyl phase, the polar group that is arranged close to the surface of silica reduces the silanol activity and improves separation of basic compound [12,13].Furthermore, various organic phases, such as macrocyclic molecules [14,15] and helical oligoamides and -peptides [16,17], achieve specific selectivity by aligning functional groups based on their steric structure.We also found that highly ordered integration of weak interaction sites such as carbonyl groups can enhance the molecular shape selectivity of a stationary phase [18,19].This was demonstrated by polymerization of carbonyl group-containing monomers and their crystallization on silica.The ordering of interaction sites in an organic phase with a simple chemical structure is an important approach to enhance molecular shape selectivity.In this work, we focus on the effect of the alignment of interaction sites in organic phases.We synthesize three types of carbonyl-containing molecular units derived from L-aspartic acid (Asp), L-glutamic acid (Glu), and L-α-aminoadipic acid (Adi) bonded to silica (Figure 1).The selected amino acids contain two carbonyl groups and have different numbers of methylene groups (x = 1, 2, and 3) between carbonyl groups.The amino acids are hydrophobized by introduction of two octadecyl alkyl chains (C n ).The number of methylene groups affects the alignment of interaction sites.The purpose of this work is to investigate the effect of interaction site alignment on the molecular shape selectivity in reversed-phase HPLC.We also examine the applicability of an amino acid derivative as an organic phase in hydrophilic interaction chromatography (HILIC) by changing the length of the alkyl chains introduced on Asp.
Separations 2016, 3, 25 2 of 11 In addition, in the case of the polar group embedded alkyl phase, the polar group that is arranged close to the surface of silica reduces the silanol activity and improves separation of basic compound [12,13].Furthermore, various organic phases, such as macrocyclic molecules [14,15] and helical oligoamides and -peptides [16,17], achieve specific selectivity by aligning functional groups based on their steric structure.We also found that highly ordered integration of weak interaction sites such as carbonyl groups can enhance the molecular shape selectivity of a stationary phase [18,19].This was demonstrated by polymerization of carbonyl group-containing monomers and their crystallization on silica.The ordering of interaction sites in an organic phase with a simple chemical structure is an important approach to enhance molecular shape selectivity.In this work, we focus on the effect of the alignment of interaction sites in organic phases.We synthesize three types of carbonyl-containing molecular units derived from L-aspartic acid (Asp), L-glutamic acid (Glu), and L-α-aminoadipic acid (Adi) bonded to silica (Figure 1).The selected amino acids contain two carbonyl groups and have different numbers of methylene groups (x = 1, 2, and 3) between carbonyl groups.The amino acids are hydrophobized by introduction of two octadecyl alkyl chains (Cn).The number of methylene groups affects the alignment of interaction sites.The purpose of this work is to investigate the effect of interaction site alignment on the molecular shape selectivity in reversed-phase HPLC.We also examine the applicability of an amino acid derivative as an organic phase in hydrophilic interaction chromatography (HILIC) by changing the length of the alkyl chains introduced on Asp.

Preparation of Amino Acid Derivatives-Bonded Stationary Phases
A typical synthetic procedure is as follows.Glu (3.00 g), stearyl alcohol (11.58 g), and p-toluenesulfonic acid monohydrate (12.02 g) as a catalyst were dispersed in toluene (100 mL).The mixture was stirred under reflux for 12 h in a flask with an attached Dean-Stark apparatus (FLAT Inc., Chiba, Japan).The solution was concentrated using an evaporator, and the residue was recrystallized from ethanol to give the p-toluenesulfonic acid salt of L-glutamic acid dioctadecylate: yield: 12.88 g (78.0%); melting point (mp): 70.6-71.4°C.Similar procedures gave the corresponding derivatives from Asp (yield: 72.3%; mp: 88.0-90.1 °C) and Adi (yield: 75.6%; mp: 79.5-80.8°C).Dimethyl esterification of Asp with thionyl chloride in methanol was also performed using a previously reported method [20].The obtained diester derivatives of the amino acids were dissolved in chloroform, neutralized with sodium hydrogen carbonate, reacted with 3isocyanatopropyltriethoxysilane (TES) as a silane-coupling agent, and recrystallized from methanol

Preparation of Amino Acid Derivatives-Bonded Stationary Phases
A typical synthetic procedure is as follows.Glu (3.00 g), stearyl alcohol (11.58 g), and p-toluenesulfonic acid monohydrate (12.02 g) as a catalyst were dispersed in toluene (100 mL).The mixture was stirred under reflux for 12 h in a flask with an attached Dean-Stark apparatus (FLAT Inc., Chiba, Japan).The solution was concentrated using an evaporator, and the residue was recrystallized from ethanol to give the p-toluenesulfonic acid salt of L-glutamic acid dioctadecylate: yield: 12.88 g (78.0%); melting point (mp): 70.6-71.4• C. Similar procedures gave the corresponding derivatives from Asp (yield: 72.3%; mp: 88.0-90.1 • C) and Adi (yield: 75.6%; mp: 79.5-80.8• C).Dimethyl esterification of Asp with thionyl chloride in methanol was also performed using a previously reported method [20].The obtained diester derivatives of the amino acids were dissolved in chloroform, neutralized with sodium hydrogen carbonate, reacted with 3-isocyanatopropyltriethoxysilane (TES) as a silane-coupling agent, and recrystallized from methanol to yield TES-Asp-2C 18 , TES-Asp-2C 1 , TES-Glu-2C 18 , and TES-Adi-2C 18 , where 2C 18 and 2C 1 correspond to dioctadecylated and dimethylated derivatives, respectively.The chemical structures of the obtained compounds were determined using 1 H nuclear magnetic resonance (NMR) and Fourier transform infrared (FT-IR) spectroscopies, and elemental analysis (EA) (See Figures S1-S11).The obtained amino acid derivatives were mixed with porous silica particles (YMC GEL SL-12S-05 silica gel, diameter 5 µm, pore size 120 Å, specific surface area 330 m 2 •g −1 ) in toluene solution under reflux for 72 h to bond on the surface of the silica particles, giving Sil-Asp-2C 18 , Sil-Asp-2C 1 , Sil-Glu-2C 18 , and Sil-Adi-2C 18 .The amounts of amino acid derivatives that bonded to silica were determined using EA and thermogravimetric analysis (TGA).

Instrumentations
EA was performed using a Micro Corder JM10 analyzer (J-Science Lab Co., Ltd., Kyoto, Japan).FT-IR spectroscopy was performed using an FT/IR-4100 instrument (JASCO, Tokyo, Japan); a DR PRO410-M accessory (JASCO, Tokyo, Japan) was used for diffuse-reflectance infrared Fourier transform (DRIFT) spectroscopy. 1H-NMR spectra were recorded using a Unity Inova AS400 spectrometer (Varian, Palo Alto, CA, USA) operating at 400 MHz.Chemical shifts are expressed in parts per million (ppm), and tetramethylsilane was used as an internal standard.Transmission electron microscopy (TEM) was performed using a JEM-2000× microscope (JEOL, Tokyo, Japan).TGA was performed using a SII Exstar 6000 TG/DTA 6300 thermobalance (SII, Chiba, Japan) in static air from 100 to 900 • C at a heating rate of 10 • C•min −1 .

Liquid Chromatography
The synthesized stationary phases were packed into stainless-steel columns that were 150 mm long with an internal diameter of 4.6 mm.A JASCO 980 pump (JASCO Corporation, Tokyo, Japan) with a Rheodyne 7725 injector (JASCO Corporation, Tokyo, Japan) (10-µL loop) and JASCO MD-2010 plus multiwavelength detector (JASCO Corporation, Tokyo, Japan) were used for liquid chromatography.The column temperature was maintained using a column jacket with a heating and cooling system.ChromNAV (version 1.14) software (JASCO Corporation, Tokyo, Japan) was used for system control and data analysis.Chromatographic-grade solvents purchased from Nacalai Tesque, Inc. (Kyoto, Japan) were used to prepare the mobile phases and samples.A commercial ODS column (GL-Science ODS-3, C: 15%, column length: 150 mm, internal diameter: 4.6 mm) (GL Science Inc., Tokyo, Japan) was used as the reference column.The retention time of methanol was used as the void volume (t 0 ) marker.The absorption of methanol was measured at 220 nm.The retention factor (k) was calculated from the retention time and t 0 .The separation factor (α) was determined as the ratio of k values.

Evaluation of the Molecular Orientation of Organic Phases
Figure 2 shows TEM images of TES-Asp-2C 18 , TES-Glu-2C 18 , and TES-Adi-2C 18 dissolved in methanol at a concentration of 0.6 mM and then cast on a carbon-coated copper grid.The amino acid derivatives formed fibrous aggregates with diameters of around 9.5 nm in methanol.This is probably because of the biphasic structure of the 2C 18 derivatives based on their non-polar properties derived from the long-chain alkyl groups, and the polar urea and ester groups.It is expected that the hydrogen bonding between the carbonyl and urea groups of the amino acid derivatives support the formation of fibrous aggregates.These results suggest that the 2C 18 derivatives can form ordered structures on the silica particle surfaces in a HPLC mobile phase such as methanol.

Bonding Density of Amino Acid Derivatives on Silica Surface
Bonding of the amino acid derivatives on the surface of silica was confirmed by DRIFT spectroscopy, EA and TGA.As illustrated in Figure 3, the DRIFT spectra of Sil-Asp-2C1, Sil-Asp-2C18, Sil-Glu-2C18 and Sil-Adi-2C18 contained peaks around 2850 and 2900 cm −1 , which are attributed to the C-H stretching of the long alkyl chains, and at 1650 and 1715 cm −1 with a shoulder at 1745 cm −1 , which are characterized as C=O vibrations of urea and ester bonds, respectively.The EA results indicate that the loading amounts of carbon in the C18-amino acid derivative-bonded silica samples were almost same as that of the reference ODS (C: 15%).This suggests that the density of alkyl chains on the silica surface was similar to that on the reference ODS.The C/N values of the samples were close to the theoretical values.No marked weight loss of the samples was observed after successive washing with good solvents such as chloroform.These results indicate that the amino acid derivatives were covalently bonded to the silica surface.The weight percentage (Pw) and surface coverage (N) of the bonded phases summarized in Table 1 were calculated from Pw (wt %) = PcM/12nC and N (μmol•m −2 ) = 10 6 Pc/[1200nc − PcM]S, where Pc is the percentage of carbon based on the EA results, S is the specific surface area of the porous silica particles used for bonding (330 m 2 •g −1 ), nc is the number of carbon atoms in a bonded molecule, and M is the molecular weight of the molecules used for bonding [21].The thermal weight loss of the stationary phases between 100 and 900 °C (Figure S12) agrees with the EA results.

Bonding Density of Amino Acid Derivatives on Silica Surface
Bonding of the amino acid derivatives on the surface of silica was confirmed by DRIFT spectroscopy, EA and TGA.As illustrated in Figure 3, the DRIFT spectra of Sil-Asp-2C 1 , Sil-Asp-2C 18 , Sil-Glu-2C 18 and Sil-Adi-2C 18 contained peaks around 2850 and 2900 cm −1 , which are attributed to the C-H stretching of the long alkyl chains, and at 1650 and 1715 cm −1 with a shoulder at 1745 cm −1 , which are characterized as C=O vibrations of urea and ester bonds, respectively.The EA results indicate that the loading amounts of carbon in the C 18 -amino acid derivative-bonded silica samples were almost same as that of the reference ODS (C: 15%).This suggests that the density of alkyl chains on the silica surface was similar to that on the reference ODS.The C/N values of the samples were close to the theoretical values.No marked weight loss of the samples was observed after successive washing with good solvents such as chloroform.These results indicate that the amino acid derivatives were covalently bonded to the silica surface.The weight percentage (P w ) and surface coverage (N) of the bonded phases summarized in Table 1 were calculated from P w (wt %) = P c M/12n C and N (µmol•m −2 ) = 10 6 P c /[1200n c − P c M]S, where P c is the percentage of carbon based on the EA results, S is the specific surface area of the porous silica particles used for bonding (330 m 2 •g −1 ), n c is the number of carbon atoms in a bonded molecule, and M is the molecular weight of the molecules used for bonding [21].The thermal weight loss of the stationary phases between 100 and 900 • C (Figure S12) agrees with the EA results.

Bonding Density of Amino Acid Derivatives on Silica Surface
Bonding of the amino acid derivatives on the surface of silica was confirmed by DRIFT spectroscopy, EA and TGA.As illustrated in Figure 3, the DRIFT spectra of Sil-Asp-2C1, Sil-Asp-2C18, Sil-Glu-2C18 and Sil-Adi-2C18 contained peaks around 2850 and 2900 cm −1 , which are attributed to the C-H stretching of the long alkyl chains, and at 1650 and 1715 cm −1 with a shoulder at 1745 cm −1 , which are characterized as C=O vibrations of urea and ester bonds, respectively.The EA results indicate that the loading amounts of carbon in the C18-amino acid derivative-bonded silica samples were almost same as that of the reference ODS (C: 15%).This suggests that the density of alkyl chains on the silica surface was similar to that on the reference ODS.The C/N values of the samples were close to the theoretical values.No marked weight loss of the samples was observed after successive washing with good solvents such as chloroform.These results indicate that the amino acid derivatives were covalently bonded to the silica surface.The weight percentage (Pw) and surface coverage (N) of the bonded phases summarized in Table 1 were calculated from Pw (wt %) = PcM/12nC and N (μmol•m −2 ) = 10 6 Pc/[1200nc − PcM]S, where Pc is the percentage of carbon based on the EA results, S is the specific surface area of the porous silica particles used for bonding (330 m 2 •g −1 ), nc is the number of carbon atoms in a bonded molecule, and M is the molecular weight of the molecules used for bonding [21].The thermal weight loss of the stationary phases between 100 and 900 °C (Figure S12) agrees with the EA results.

Reversed Phase Liquid Chromatography
Chromatographic separations were performed with the Sil-Asp-2C 18 , Sil-Glu-2C 18 and Sil-Adi-2C 18 columns (C 18 -amino acid derivative columns) using long-chain alkylated benzene derivatives and PAHs as solutes and methanol/water (9:1) as the mobile phase.With this sample set, the elution order of C18-amino acid derivative columns followed log P values of analytes (see Figure S13).In contrast, unique separation behaviors were observed when the analytes were PAHs with characteristic structures.The molecular shape selectivity of ODS is affected by the density of alkyl chains [22].The elution order of phenanthro [3,4- c]phenanthrene (PhPh), 1,2:3,4:5,6:7,8-tetrabenzonaphthalene (TBN), and benzo[a]pyrene (BaP) with monomeric ODS (C: 15%) is BaP ≤ PhPh < TBN, and with highly carbon loaded polymeric ODS (C: 30%) is PhPh ≤ TBN < BaP [22].The elution orders of prepared stationary phases were different from both ODS (PhPh < BaP < TBN, see Figure 4).Because the C18 amino acid derivatives were self-assemble molecules, there were possibilities that C18 amino acid derivatives were bonded on the surface of silica particles locally and densely.It was supposed that the assembled structure affect for the molecular recognition.To investigate this in further detail, we clarified the molecular shape selectivities of the C 18 -amino acid derivative columns using geometric isomers (cis-/trans-stilbenes), positional isomers with different twist angles (o-, m-, and p-terphenyls), and a planar compound (triphenylene), as analytes.The data in Table 2 reveal that the C 18 -amino acid derivative columns showed higher selectivity toward planar molecules than ODS did.Sil-Glu-2C 18 showed the highest selectivity for pand o-terphenyls (α = 2.46, 2.39 and 2.03 for Sil-Glu-2C 18 , Sil-Asp-2C 18 and Sil-Adi-2C 18 , respectively), but its selectivity for triphenylene and o-terphenyls was lower than those of Sil-Asp-2C 18 and Sil-Adi-2C 18 (α = 2.72, 3.81 and 2.99 for Sil-Glu-2C 18 , Sil-Asp-2C 18 and Sil-Adi-2C 18 , respectively).The length-to-breadth ratio (L/B) [23,24] is a useful indicator for evaluating molecular shape.In this work, four planar PAHs, triphenylene (L/B = 1.12), benz[a]anthracene (L/B = 1.58), chrysene (L/B = 1.72), and naphthacene (L/B = 1.89), were selected to investigate the molecular shape selectivity of the C 18 -amino acid derivative columns.Determination of the selectivities of the columns for these molecules showed that the stationary phases with bonded C 18 -amino acid derivatives selectively recognized molecules with higher L/B values.The naphthacene/triphenylene separation factors were the highest and lowest for Sil-Asp-2C 18 and Sil-Glu-2C 18 , respectively.We also evaluated the selectivity of Sil-Asp-2C 1 using PAHs, as summarized in Table 2.    Mobile phase: methanol-water (9:1), flow rate: 1.0 mL•min −1 , column temperature: 20 °C.The α values were calculated using the k of the first analyte and others respectively, in each group.Mobile phase: methanol-water (9:1), flow rate: 1.0 mL•min −1 , column temperature: 20 °C.The α values were calculated using the k of the first analyte and others respectively, in each group.Mobile phase: methanol-water (9:1), flow rate: 1.0 mL•min −1 , column temperature: 20 °C.The α values were calculated using the k of the first analyte and others respectively, in each group.
To further investigate the C18-amino acid derivative columns, temperature dependencies of the  Mobile phase: methanol-water (9:1), flow rate: 1.0 mL•min −1 , column temperature: 20 °C.The α values were calculated using the k of the first analyte and others respectively, in each group.
To further investigate the C18-amino acid derivative columns, temperature dependencies of the selectivities for triphenylene/o-terphenyl (αtriph/o-terp) and naphthacene/triphenylene (αnaph/triph) were evaluated.Figure 5 reveals that a linear plot was observed for ODS.In contrast, bending points were  Mobile phase: methanol-water (9:1), flow rate: 1.0 mL•min −1 , column temperature: 20 °C.The α values were calculated using the k of the first analyte and others respectively, in each group.
To further investigate the C18-amino acid derivative columns, temperature dependencies of the selectivities for triphenylene/o-terphenyl (αtriph/o-terp) and naphthacene/triphenylene (αnaph/triph) were evaluated.Figure 5 reveals that a linear plot was observed for ODS.In contrast, bending points were observed in the plots of C18-amino acid derivative columns.This suggests that a steric structure  Mobile phase: methanol-water (9:1), flow rate: 1.0 mL•min −1 , column temperature: 20 °C.The α values were calculated using the k of the first analyte and others respectively, in each group.
To further investigate the C18-amino acid derivative columns, temperature dependencies of the selectivities for triphenylene/o-terphenyl (αtriph/o-terp) and naphthacene/triphenylene (αnaph/triph) were evaluated.Figure 5 reveals that a linear plot was observed for ODS.In contrast, bending points were observed in the plots of C18-amino acid derivative columns.This suggests that a steric structure  Mobile phase: methanol-water (9:1), flow rate: 1.0 mL•min −1 , column temperature: 20 °C.The α values were calculated using the k of the first analyte and others respectively, in each group.
To further investigate the C18-amino acid derivative columns, temperature dependencies of the selectivities for triphenylene/o-terphenyl (αtriph/o-terp) and naphthacene/triphenylene (αnaph/triph) were evaluated.Figure 5 reveals that a linear plot was observed for ODS.In contrast, bending points were observed in the plots of C18-amino acid derivative columns.This suggests that a steric structure  Mobile phase: methanol-water (9:1), flow rate: 1.0 mL•min −1 , column temperature: 20 °C.The α values were calculated using the k of the first analyte and others respectively, in each group.
To further investigate the C18-amino acid derivative columns, temperature dependencies of the selectivities for triphenylene/o-terphenyl (αtriph/o-terp) and naphthacene/triphenylene (αnaph/triph) were evaluated.Figure 5 reveals that a linear plot was observed for ODS.In contrast, bending points were observed in the plots of C18-amino acid derivative columns.This suggests that a steric structure To further investigate the C 18 -amino acid derivative columns, temperature dependencies of the selectivities for triphenylene/o-terphenyl (α triph/o-terp ) and naphthacene/triphenylene (α naph/triph ) were evaluated.Figure 5 reveals that a linear plot was observed for ODS.In contrast, bending points were observed in the plots of C 18 -amino acid derivative columns.This suggests that a steric structure change related to the molecular interaction occurred on the stationary phase.Moreover, the higher selectivities of the C 18 -amino acid derivative columns at temperatures below 25 • C are related to temperature-dependent molecular ordering.The ordering of the molecules on the surface of the stationary phase indicates that the organic phases are locally densely bonded.This is one of the reasons for the unique selectivity of the C 18 -amino acid derivative columns.The aligned carbonyl groups may also contribute to the molecular shape selectivity of the C 18 -amino acid derivative columns.The number of methylene groups between the carbonyl groups of the C 18 -amino acid derivatives is odd except for in the Glu derivative.Because of this, it is presumed that the configuration of carbonyl groups in the Glu derivative is obviously different from that of the other amino acid derivatives.The alignment of the interaction sites on Sil-Glu-2C 18 therefore must differs from those of the other amino acid derivatives, when it orientates on the surface of silica, and promotes recognition of the twisted structures of terphenyl isomers.For the same reason, the alignments of the interaction sites in Sil-Asp-2C 18 and Sil-Adi-2C 18 are better for recognition of planar and linear molecules than that in Sil-Glu-2C 18 .

Hydrophilic Interaction Chromatography
The applicability of an amino acid derivative-bonded stationary phase to HILIC mode was evaluated using Sil-Asp-2C1.The typical HILIC mode retention order was observed for phenol, resorcinol, and phloroglucinol with Sil-Asp-2C1: higher k value was achieved by increasing the number of hydroxyl groups of the analyte (Table S1) [25].Usually, a mixture of water and a polar organic solvent such as acetonitrile is used for the mobile phase in HILIC.The retention mechanism of HILIC involves liquid-liquid partitioning between the mobile phase and absorbed water on the surface of the stationary phase [26].Thus, by increasing the content of water in the mobile phase, the retention in HILIC will decrease.Figure 6 shows the relationship between k and the proportion of acetonitrile in the mobile phase.Decreasing the content of acetonitrile in the mobile phase decreased the k values of all selected polar molecules, which is consistent with the usual retention behavior in HILIC.This is the typical HILIC mode retention behavior [25,27].In addition, larger k values were obtained by molecules that show lower pKa values (e.g., pKa = 4.2 and 4.2 for adenine and cytosine [28]) among a sample set (e.g., pKa = 10.5 for thymine [28]).In the HILIC, in addition to the partitioning, ion exchange between positively charged molecules and negative charged silanol also affected the retentivity.This effect may be revealed in this study.

Hydrophilic Interaction Chromatography
The applicability of an amino acid derivative-bonded stationary phase to HILIC mode was evaluated using Sil-Asp-2C 1 .The typical HILIC mode retention order was observed for phenol, resorcinol, and phloroglucinol with Sil-Asp-2C 1 : higher k value was achieved by increasing the number of hydroxyl groups of the (Table S1) [25].Usually, a mixture of water and a polar organic solvent such as acetonitrile is used for the mobile phase in HILIC.The retention mechanism of HILIC involves liquid-liquid partitioning between the mobile phase and absorbed water on the surface of the stationary phase [26].Thus, by increasing the content of water in the mobile phase, the retention in HILIC will decrease.Figure 6 shows the relationship between k and the proportion of acetonitrile in the mobile phase.Decreasing the content of acetonitrile in the mobile phase decreased the k values of all selected polar molecules, which is consistent with the usual retention behavior in HILIC.This is the typical HILIC mode retention behavior [25,27].In addition, larger k values were obtained by molecules that show lower pKa values (e.g., pKa = 4.2 and 4.2 for adenine and cytosine [28]) among a sample set (e.g., pKa = 10.5 for thymine [28]).In the HILIC, in addition to the partitioning, ion exchange between positively charged molecules and negative charged silanol also affected the retentivity.This effect may be revealed in this study.organic solvent such as acetonitrile is used for the mobile phase in HILIC.The retention mechanism of HILIC involves liquid-liquid partitioning between the mobile phase and absorbed water on the surface of the stationary phase [26].Thus, by increasing the content of water in the mobile phase, the retention in HILIC will decrease.Figure 6 shows the relationship between k and the proportion of acetonitrile in the mobile phase.Decreasing the content of acetonitrile in the mobile phase decreased the k values of all selected polar molecules, which is consistent with the usual retention behavior in HILIC.This is the typical HILIC mode retention behavior [25,27].In addition, larger k values were obtained by molecules that show lower pKa values (e.g., pKa = 4.2 and 4.2 for adenine and cytosine [28]) among a sample set (e.g., pKa = 10.5 for thymine [28]).In the HILIC, in addition to the partitioning, ion exchange between positively charged molecules and negative charged silanol also affected the retentivity.This effect may be revealed in this study.These results suggest that weak interaction site accumulation based on amino acids has the potential for application in molecular design for HILIC.

Separation of Tocopherol Isomers
Practical applications of the C 18 -amino acid derivative columns were evaluated using the tocopherol isomers (α, β, γ, and δ isomers).Tocopherols are hydrophobic vitamins that have many beneficial bioeffects such as antioxidant and anti-inflammatory properties.For example, the importance of the role of tocopherols in retinal precursor cell differentiation is being increasingly studied [29].Figure 7 depicts chromatograms of tocopherols obtained using the C 18 -amino acid derivative columns and ODS.Separation of the β and γ isomers was not achieved using ODS, but was realized using the stationary phases with bonded octadecylated amino acid derivatives.In particular, Sil-Asp-2C 18 successfully separated all the isomers in the reversed-phase mode.These results suggest that weak interaction site accumulation based on amino acids has the potential for application in molecular design for HILIC.

Separation of Tocopherol Isomers
Practical applications of the C18-amino acid derivative columns were evaluated using the tocopherol isomers (α, β, γ, and δ isomers).Tocopherols are hydrophobic vitamins that have many beneficial bioeffects such as antioxidant and anti-inflammatory properties.For example, the importance of the role of tocopherols in retinal precursor cell differentiation is being increasingly studied [29].Figure 7 depicts chromatograms of tocopherols obtained using the C18-amino acid derivative columns and ODS.Separation of the β and γ isomers was not achieved using ODS, but was realized using the stationary phases with bonded octadecylated amino acid derivatives.In particular, Sil-Asp-2C18 successfully separated all the isomers in the reversed-phase mode.

Conclusions
Organic stationary phases based on Asp, Glu, and Adi with aligned carbonyl groups were synthesized and bonded on silica particles.These stationary phases showed higher molecular shape selectivities for PAHs than ODS.The highest selectivity for p-/o-terphenyl and naphthacene/oterphenyl were obtained by Sil-Glu-2C18 and Sil-Asp-2C18, respectively.Sil-Asp-2C18, Sil-Glu-2C18, and Sil-Adi-2C18 differ in the number of methylene groups between carbonyl groups in the original amino acids; therefore, these results indicate that the alignment of the carbonyl groups as interaction

Figure 1 .
Figure 1.Chemical structures of amino acid derivative-bonded stationary phases.

Figure 1 .
Figure 1.Chemical structures of amino acid derivative-bonded stationary phases.

Table 2 .
Retention and separation factors (k and α) with C 18 -amino acid derivative columns.
Mobile phase: methanol-water (9:1), flow rate: 1.0 mL•min −1 , column temperature: 20 • C. The α values were calculated using the k of the first analyte and others respectively, in each group.

Figure 6 .
Figure 6.Effect of acetonitrile content ratio on the retention factors of polar molecules with Sil-Asp-2C1.Mobile phase: acetonitrile and 10 mM ammonium acetate mixture, flow rate: 1.0 mL•min −1 , column temperature: 10 °C.

Table 2 .
Retention and separation factors (k and α) with C18-amino acid derivative columns.

Table 2 .
Retention and separation factors (k and α) with C18-amino acid derivative columns.

Table 2 .
Retention and separation factors (k and α) with C18-amino acid derivative columns.

Table 2 .
Retention and separation factors (k and α) with C18-amino acid derivative columns.

Table 2 .
Retention and separation factors (k and α) with C18-amino acid derivative columns.

Table 2 .
Retention and separation factors (k and α) with C18-amino acid derivative columns.

Table 2 .
Retention and separation factors (k and α) with C18-amino acid derivative columns.

Table 2 .
Retention and separation factors (k and α) with C18-amino acid derivative columns.

Table 2 .
Retention and separation factors (k and α) with C18-amino acid derivative columns.

Table 2 .
Retention and separation factors (k and α) with C18-amino acid derivative columns.