Microporous Materials Based on Norbornadiene-Based Cross-Linked Polymers

New microporous homopolymers were readily prepared from norbornadiene-2,5, its dimer and trimer by addition (vinyl) polymerization of the corresponding monomers with 60–98% yields. As a catalyst Pd-N-heterocyclic carbene complex or Ni(II) 2-ethylhexanoate activated with Na+[B(3,5-(CF3)2C6H3)4]− or methylaluminoxane was used. The synthesized polynorbornenes are cross-linked and insoluble. They are glassy and amorphous polymers. Depending on the nature of the catalyst applied, BET surface areas were in the range of 420–970 m2/g. The polymers with the highest surface area were obtained in the presence of Pd-catalysts from the trimer of norbornadiene-2,5. The total pore volume of the polymers varies from 0.39 to 0.79 cm3/g, while the true volume of micropores was 0.14–0.16 cm3/g according to t-plot. These polymers gave CO2 uptake from 1.2 to 1.9 mmol/g at 273 K and 1 atm. The porous structure of new polymers was also studied by means of wide-angle X-ray diffraction and positron annihilation lifetime spectroscopy.


Introduction
Microporous materials are attractive materials for gas storage, heterogeneous catalysis, membrane gas separation and so on. Crystalline zeolites and amorphous activated carbons are the most known examples of such materials. However, their opportunities (e.g., for hydrogen and hydrocarbon storage) are limited, therefore, the design of new microporous materials is a problem. In recent decades, a wide range of such materials with different properties have been developed [1,2]. For example, metal-organic frameworks (MOFs) and covalent-organic frameworks (COFs) possess crystalline order and narrow pore size distribution, hence, they are organic analogues of zeolites [3,4]. Another example is amorphous porous polymeric materials, for instance rigid-chain linear polymers such as TR-polymers [7], ferrocene-based polymers [8], polynorbornenes [9,10], and network polymers, such as cross-linked PIMs [11], aromatic conjugated microporous polymers [12] and polyolefins [13]. These polymers possess high surface areas and wide synthetic opportunities for modifications, and are therefore of great interest as membranes or gas storage materials. Polynorbornenes are of particular interest because of several advantages. Firstly, norbornenes could be easily modified which makes possible the introduction of a wide range of substituents within polymers. Secondly, norbornenes are capable of being polymerized by different mechanisms (metathesis [14], addition [15,16] or isomerization [17,18] polymerization), which results in polymers with a different main chain structure and chain rigidity, and hence various properties. This makes polynorbornenes attractive to design new polymers with desired properties [19,20]. Earlier we have shown that Me3Si-substituted addition polynorbornenes, being rigid-chain linear polymers, possess BET (obtained by Brunauer-Emmett-Teller method) surface area up to 780 m 2 /g, and are promising materials for membrane gas separation of hydrocarbons or CO2/N2 because of their extremely high gas permeability and/or high separation selectivities [21][22][23]. Herein we report the synthesis and properties of novel network amorphous porous polymers based on bifunctional norbornene monomers, namely norborbornadiene-2,5 and its oligomers ( Figure 1). These monomers are more synthetically available than earlier studied silicon-substituted norbornenes, and the presence of two double bonds in them allows for creating various branched and network porous polymer structures depending on polymerization conditions and the size of monomer (the distance between double bonds in a monomer influences the length of cross-linkages). So, their polymerization could provide a simple approach to new microporous organic materials for various applications, especially gas storage and as fillers for modifications of gas separation composite membranes.
Characteristics of the porous structure of polymers were determined by nitrogen (77 K) and carbon dioxide (273 K) adsorption using a Gemini VIIt analyzer (Micromeritics Instrument Corporation, Norcross, GA, USA). All the samples were degassed at 100 °C at 25-50 mTorr for 10 h before measurements. Surface area was calculated by BET (N2) and Langmuir (CO2) equations. The
Characteristics of the porous structure of polymers were determined by nitrogen (77 K) and carbon dioxide (273 K) adsorption using a Gemini VIIt analyzer (Micromeritics Instrument Corporation, Norcross, GA, USA). All the samples were degassed at 100 • C at 25-50 mTorr for 10 h Polymers 2018, 10, 1382 3 of 16 before measurements. Surface area was calculated by BET (N 2 ) and Langmuir (CO 2 ) equations. The calculations of S BET were performed in the range of relative pressure (p/p 0 ) of 0.08-0.22 in the case of polyDNBD synthesized over Ni-catalyst, and 0.03-0.15 in all other cases. Mesopores size distribution were calculated using the BJH (Barrett-Joyner-Halenda) method. The Harkins-Jura equation was used for adsorption film thickness calculation. Micropore volume and surface were determined using the Dubinin equation. Micropore size distribution was estimated using the Horvath-Kawazoe method.
The T-plot method was used for external surface area and micropore volume value calculation.
The concentration of double bonds in polymers was measured by ozonation method on the compact original device "Double Bonds Analyzer" (DBA) which has ozone sensitivity on 10 −8 mol/L, precision up to 0.1 % and short analysis time from 1 to 2 min [27].
The amount of double bonds in polyDNBD was also estimated by IR spectroscopy. The intensities of peaks at 3066 or 1562 cm −1 relative to the intensity of peak at 1451 cm −1 for polymers were compared with corresponding values for the monomer (see Figure S1).

Positron Annihilation Lifetime Spectroscopy (PALS)
The positron annihilation lifetime decay curves were measured at room temperature using an EG@GOrtec "fast-fast" lifetime spectrometer. A nickel-foil-supported [ 44 Ti] radioactive positron source was used. Two stacks of film samples, each with a total thickness of about 1 mm, were placed on either side of the source. All the measurements were performed in inert (nitrogen) atmosphere. The time resolution was 300 ps (full width at the halfmaximum (fwhm) of the prompt coincidence curve). The contribution from annihilation in the source material, a background, and instrumental resolution were taken into account in the PATFIT program for treating the experimental lifetime data. The resulting data were determined as an average value from the several spectra collected for the same sample, having an integral number of counts of at least 10 6 in each spectrum.
PALS is based on the measurements of positron lifetime spectra in polymers-lifetimes τ i (ns) and corresponding intensities I i (%). Longer lifetimes τ 3 and τ 4 can be related to the mean size of free volume elements (FVE) in polymers according to the Tao-Eldrup formula: [28,29] where τ i = τ 3 or τ 4 are o-Ps lifetimes and R i = R 3 or R 4 are the radii of free volume elements expressed in nanoseconds and angstroms respectively; λ T 0 -stands for the intrinsic ortho-Ps annihilation rate (0.7·10 9 s −1 ); ∆R = 1.66 Å is the fitted empirical parameter.

Hydrogenation of Addition PolyDNBD
PolyDNBD (0.2 g, 1.1 mmol monomer units) and p-toluenesulfonyl hydrazide (1.4 g, 7.5 mmol) were charged to a two-necked flask equipped with a magnetic stirrer and reflux condenser. The flask was evacuated and filled with argon. Then 10 mL of absolute o-xylene were added to the flask, and the mixture was refluxed for 15 h. The precipitate was isolated, soxhleted with chloroform for 3 h, and dried in vacuum at 40-60 • C up to a constant weight. Yield: 0.176 g (88 %). 13

Synthesis of Polymers
Since norbornadiene-2,5 and its oligomers are bifunctional monomers (they have two polymerizable norbornene double bonds), their polymerization results in the formation of insoluble network polymers. These monomers proved to be highly reactive in metathesis and addition polymerization (Scheme 1). Metathesis polymerization of DNBD was conducted in the presence of the 1st generation Grubbs catalyst leading to a glassy (T g was higher than the decomposition temperature) and amorphous polymer in a good yield ( Table 1). The polymer formed turned out to possess low BET surface area (<10 m 2 /g, see below). Therefore, further investigations of metathesis polymers based on NBD and its oligomers were not performed.  Monomer concentration in the reaction mixture. 3 The amount of norbornene double bonds in the polymer per monomer unit estimated by IR spectroscopy. 4 The amount of double bonds per monomer unit estimated by ozonation method.
Addition polymerization of DNBD was carried out in the presence of Pd-and Ni-based catalytic systems. As a Pd-catalytic system Pd-N-heterocyclic carbene complex (SIPrPd(cinn)Cl, Scheme 1) in combination with NaBARF and tricyclohexylphosphine was applied as one of the most active and stable catalysts in addition polymerization [23,30]. Nickel ethylhexanoate in combination with NaBARF and methylaluminoxane was used as a readily available Ni-based system for addition polymerization. It was found that there is a difference in the process of a polymer formation between polymerizations in the presence of Pd-and Ni-based catalysts. In the case of the former, a few minutes after the initiation a solid precipitate formed, while in the case of the latter a gel formed. Nevertheless, NMR spectra of addition polymers prepared from DNBD in the presence of different catalysts are similar ( Figure 2) indicating a close microstructure. Addition homopolymers based on NBD and TNBD were synthesized also using the similar Pd-based catalyst. NBD was as reactive as Scheme 1. Metathesis and addition polymerization of NBD and its oligomers.  3 The amount of norbornene double bonds in the polymer per monomer unit estimated by IR spectroscopy. 4 The amount of double bonds per monomer unit estimated by ozonation method.
Addition polymerization of DNBD was carried out in the presence of Pd-and Ni-based catalytic systems. As a Pd-catalytic system Pd-N-heterocyclic carbene complex (SIPrPd(cinn)Cl, Scheme 1) in combination with NaBARF and tricyclohexylphosphine was applied as one of the most active and stable catalysts in addition polymerization [23,30]. Nickel ethylhexanoate in combination with NaBARF and methylaluminoxane was used as a readily available Ni-based system for addition polymerization. It was found that there is a difference in the process of a polymer formation between polymerizations in the presence of Pd-and Ni-based catalysts. In the case of the former, a few minutes after the initiation a solid precipitate formed, while in the case of the latter a gel formed. Nevertheless, NMR spectra of addition polymers prepared from DNBD in the presence of different catalysts are similar ( Figure 2) indicating a close microstructure. Addition homopolymers based on NBD and TNBD were synthesized also using the similar Pd-based catalyst. NBD was as reactive as DNBD, but its polymerization gave some soluble oligomeric fraction (up to 40 mass. %) separated out at the purification stage along with the formation of the insoluble network polymer. The polymerization of TNBD was complicated by its lower solubility in 1,2-dichloroethane (0.13 g/mL) in comparison with DNBD (1.2 g/mL) and as a result the polymerization was performed in more diluted solutions using toluene as a solvent.
Polymers 2018, 10, x FOR PEER REVIEW 6 of 16 DNBD, but its polymerization gave some soluble oligomeric fraction (up to 40 mass. %) separated out at the purification stage along with the formation of the insoluble network polymer. The polymerization of TNBD was complicated by its lower solubility in 1,2-dichloroethane (0.13 g/mL) in comparison with DNBD (1.2 g/mL) and as a result the polymerization was performed in more diluted solutions using toluene as a solvent.    The structure of synthesized homopolymers was examined by CP/MAS NMR ( Figure 2) and IR spectroscopy ( Figure S1). Despite the fact that addition polymerization results in structures with the saturated nature of main chains, the addition polymers from NBD and its oligomers proved to contain double bonds. This means that not all double bonds were involved in addition polymerization. The amount of double bonds in polymers estimated by ozonation correlates with the monomer size and grows in the row polyNBD < polyDNBD < polyTNBD (Table 1). IR spectra of polymers after ozonation are shown in Figure S2. The amount of double bonds in polyDNBD was estimated by IR spectroscopy and it depended on the nature of catalyst used to obtain the polymer ( Table 1). The fully saturated polymers could be readily obtained by the hydrogenation of the polymers formed in addition polymerization. Thus, the hydrogenation of polyDNBD synthesized using Pd-catalyst was done with tosyl hydrazide (Scheme 2). All double bonds were hydrogenated, that was confirmed by 13 C CP/MAS NMR spectroscopy (Figure 2). The structure of synthesized homopolymers was examined by CP/MAS NMR ( Figure 2) and IR spectroscopy ( Figure S1). Despite the fact that addition polymerization results in structures with the saturated nature of main chains, the addition polymers from NBD and its oligomers proved to contain double bonds. This means that not all double bonds were involved in addition polymerization. The amount of double bonds in polymers estimated by ozonation correlates with the monomer size and grows in the row polyNBD < polyDNBD < polyTNBD (Table 1). IR spectra of polymers after ozonation are shown in Figure S2. The amount of double bonds in polyDNBD was estimated by IR spectroscopy and it depended on the nature of catalyst used to obtain the polymer ( Table 1). The fully saturated polymers could be readily obtained by the hydrogenation of the polymers formed in addition polymerization. Thus, the hydrogenation of polyDNBD synthesized using Pd-catalyst was done with tosyl hydrazide (Scheme 2). All double bonds were hydrogenated, that was confirmed by 13 C CP/MAS NMR spectroscopy (Figure 2). The surface morphology of polyDNBD-es synthesized over Pd-and Ni-catalyst was observed by SEM (Figure 3). Unlike solid polymer synthesized using Ni-catalyst, the polymer synthesized over Pd-catalyst, being a powder, consist of the aggregates of particles with the size of less than 1 μm.

WAXD and TGA Characterization of the Synthesized Polymers
All synthesized addition homopolymers proved to be amorphous ( Figure 4). According to WAXD data polyTNBD has the larger d-spacing than polyDNBD, which is indicated by a peak shifted at the smaller 2θ angle (Table 3). At the same time addition polyDNBD-es obtained over different catalysts differ by d-spacing values: the corresponding value for polyDNBD obtained in the presence of Pd-catalyst is higher than that for polyDNBD prepared over Ni-catalyst. This difference in d-spacing distances and a more diffused WAXD pattern of addition polyDNBD synthesized with The surface morphology of polyDNBD-es synthesized over Pd-and Ni-catalyst was observed by SEM ( Figure 3). Unlike solid polymer synthesized using Ni-catalyst, the polymer synthesized over Pd-catalyst, being a powder, consist of the aggregates of particles with the size of less than 1 µm. The structure of synthesized homopolymers was examined by CP/MAS NMR ( Figure 2) and IR spectroscopy ( Figure S1). Despite the fact that addition polymerization results in structures with the saturated nature of main chains, the addition polymers from NBD and its oligomers proved to contain double bonds. This means that not all double bonds were involved in addition polymerization. The amount of double bonds in polymers estimated by ozonation correlates with the monomer size and grows in the row polyNBD < polyDNBD < polyTNBD (Table 1). IR spectra of polymers after ozonation are shown in Figure S2. The amount of double bonds in polyDNBD was estimated by IR spectroscopy and it depended on the nature of catalyst used to obtain the polymer ( Table 1). The fully saturated polymers could be readily obtained by the hydrogenation of the polymers formed in addition polymerization. Thus, the hydrogenation of polyDNBD synthesized using Pd-catalyst was done with tosyl hydrazide (Scheme 2). All double bonds were hydrogenated, that was confirmed by 13 C CP/MAS NMR spectroscopy (Figure 2). The surface morphology of polyDNBD-es synthesized over Pd-and Ni-catalyst was observed by SEM (Figure 3). Unlike solid polymer synthesized using Ni-catalyst, the polymer synthesized over Pd-catalyst, being a powder, consist of the aggregates of particles with the size of less than 1 μm.

WAXD and TGA Characterization of the Synthesized Polymers
All synthesized addition homopolymers proved to be amorphous ( Figure 4). According to WAXD data polyTNBD has the larger d-spacing than polyDNBD, which is indicated by a peak shifted at the smaller 2θ angle (Table 3). At the same time addition polyDNBD-es obtained over different catalysts differ by d-spacing values: the corresponding value for polyDNBD obtained in the presence of Pd-catalyst is higher than that for polyDNBD prepared over Ni-catalyst. This difference in d-spacing distances and a more diffused WAXD pattern of addition polyDNBD synthesized with

WAXD and TGA Characterization of the Synthesized Polymers
All synthesized addition homopolymers proved to be amorphous (Figure 4). According to WAXD data polyTNBD has the larger d-spacing than polyDNBD, which is indicated by a peak shifted at the smaller 2θ angle (Table 3). At the same time addition polyDNBD-es obtained over different catalysts differ by d-spacing values: the corresponding value for polyDNBD obtained in the presence of Pd-catalyst is higher than that for polyDNBD prepared over Ni-catalyst. This difference in d-spacing distances and a more diffused WAXD pattern of addition polyDNBD synthesized with Ni-catalyst Ni-catalyst clearly indicate different chain packing of polyDNBD polymers obtained over various catalysts. Hydrogenation of polyDNBD led to a polymer with larger d-spacing distances in comparison with the d-spacing values for the initial unsaturated polymer and it could be concluded that the hydrogenated polyDNBD has larger free volume and a more porous structure.  The prepared polymers exhibited high thermal stability under an inert atmosphere (up to 386 °C for 5 % mass loss, Figure 5). In the TGA curve of polyDNBD in air, an increase of the sample mass was revealed at 220-300 °C, which indicated the oxidation of double bonds (see IR spectra in Figure  S3). This observation is in contrast to the thermal properties of metathesis polynorbornenes containing internal double bonds in main chains: for them the increase of mass sample was not found in TGA curves in air. This difference is evidence that double bonds in the synthesized polymers are available and they can be readily modified leading to new polymers. The prepared polymers exhibited high thermal stability under an inert atmosphere (up to 386 • C for 5 % mass loss, Figure 5). In the TGA curve of polyDNBD in air, an increase of the sample mass was revealed at 220-300 • C, which indicated the oxidation of double bonds (see IR spectra in Figure S3). This observation is in contrast to the thermal properties of metathesis polynorbornenes containing internal double bonds in main chains: for them the increase of mass sample was not found in TGA curves in air. This difference is evidence that double bonds in the synthesized polymers are available and they can be readily modified leading to new polymers.

Positron Annihilation Lifetime Spectroscopy (PALS) Study
Interesting results concerning free volume distribution in a polymer were obtained from the analysis of the prepared addition polymers by positron annihilation lifetime spectroscopy (PALS). It was found that in the synthesized polyDNBD, the intensity of smaller free volume elements (I3) is

Positron Annihilation Lifetime Spectroscopy (PALS) Study
Interesting results concerning free volume distribution in a polymer were obtained from the analysis of the prepared addition polymers by positron annihilation lifetime spectroscopy (PALS). It was found that in the synthesized polyDNBD, the intensity of smaller free volume elements (I 3 ) is significantly higher than larger ones (Table 2), in contrast to earlier studied microporous Si-containing addition polynorbornenes [21,22]. At the same time, the intensity of larger free volume elements is very low. The size of free volume elements (R 3 and R 4 ) is comparable with earlier studied related microporous polynorbornenes [9]. These data are evidence that the prepared addition polymers from NBD and its oligomers possess narrower pore size distribution.  Figure 5. TGA curves of addition polymers from NBD and its oligomers synthesized using Pd-catalyst.

Positron Annihilation Lifetime Spectroscopy (PALS) Study
Interesting results concerning free volume distribution in a polymer were obtained from the analysis of the prepared addition polymers by positron annihilation lifetime spectroscopy (PALS). It was found that in the synthesized polyDNBD, the intensity of smaller free volume elements (I3) is significantly higher than larger ones (Table 2), in contrast to earlier studied microporous Si-containing addition polynorbornenes [21,22]. At the same time, the intensity of larger free volume elements is very low. The size of free volume elements (R3 and R4) is comparable with earlier studied related microporous polynorbornenes [9]. These data are evidence that the prepared addition polymers from NBD and its oligomers possess narrower pore size distribution.  Figure 5. TGA curves of addition polymers from NBD and its oligomers synthesized using Pd-catalyst.

Positron Annihilation Lifetime Spectroscopy (PALS) Study
Interesting results concerning free volume distribution in a polymer were obtained from the analysis of the prepared addition polymers by positron annihilation lifetime spectroscopy (PALS). It was found that in the synthesized polyDNBD, the intensity of smaller free volume elements (I3) is significantly higher than larger ones (Table 2), in contrast to earlier studied microporous Si-containing addition polynorbornenes [21,22]. At the same time, the intensity of larger free volume elements is very low. The size of free volume elements (R3 and R4) is comparable with earlier studied related microporous polynorbornenes [9]. These data are evidence that the prepared addition polymers from NBD and its oligomers possess narrower pore size distribution.  Figure 5. TGA curves of addition polymers from NBD and its oligomers synthesized using Pd-catalyst.

Positron Annihilation Lifetime Spectroscopy (PALS) Study
Interesting results concerning free volume distribution in a polymer were obtained from the analysis of the prepared addition polymers by positron annihilation lifetime spectroscopy (PALS). It was found that in the synthesized polyDNBD, the intensity of smaller free volume elements (I3) is significantly higher than larger ones (Table 2), in contrast to earlier studied microporous Si-containing addition polynorbornenes [21,22]. At the same time, the intensity of larger free volume elements is very low. The size of free volume elements (R3 and R4) is comparable with earlier studied related microporous polynorbornenes [9]. These data are evidence that the prepared addition polymers from NBD and its oligomers possess narrower pore size distribution.

N 2 and CO 2 Adsorption Studies
The characteristics of the porous structure of synthesized polymers was evaluated by low temperature nitrogen and CO 2 adsorption. Figure 6 and Figure S4 show some adsorption-desorption isotherms of nitrogen for addition polymers from NBD and its oligomers. The shape of isotherms for these polymers is similar to type IV, while the hysteresis loop belongs to H3 type. In the case of all addition polymers prepared herein over Pd-catalyst, there is a high uptake of nitrogen even at low relative pressure. This indicates the presence of micropores for these polymers. At the same time, no microporosity was found for polyDNBD obtained using Ni-catalyst. This polymer was a mesoporous material. Thus, the nature of a catalyst determines the free volume architecture in the considered polymers.
The synthesized addition polymers possess high BET surface area (up to 420-970 m 2 /g, Table 3). The value of BET surface area for the obtained addition polymers depends on the nature of a monomer and the conditions of polymerization. Thus, the highest value was found for the addition polymer from TNBD. This monomer provides the longest interchain linkages within the cross-linked addition polymers based on NBD, its dimer or trimer. It should be noted that, to the best of our knowledge, the value of BET surface area reached in the case of addition polymer from trimer of NBD is the highest one among the values for any polynorbornenes reported so far [16]. The values obtained for specific surface areas are also much higher than a recently reported value for another addition polynorbornene from dicyclopentadiene (S BET = 155 m 2 /g) [10]. This difference can be explained by the presence of a bulkier bicyclic group in the monomer and the formation of cross-links during the polymerization, which stabilize the porous architecture of the formed polymers. BET surface area values for the synthesized polymers are close or higher than corresponding values obtained for some other microporous polymers (like PIM-1, PTMSP and TR-polymers) displaying promising properties for membrane gas separation ( Table 3). The decrease of the distance between two double bonds in a bifunctional norbornene led to lower BET surface area of the formed addition homopolymers based on these monomers. For example, addition polyDNBD displayed S BET as high as 730 m 2 /g. Hydrogenation of the obtained polymers resulted in a noticeable increase of surface area. The synthesis of polymers from NBD and its oligomers in more diluted solutions led to the materials with a little higher BET surface area. This is probably explained by higher conversions of both double bonds of bifunctional NBD oligomers in more diluted solutions. The nature of a catalyst used for a polymer synthesis exerts a stronger influence on porosity of the formed polymers. For instance, for polyDNBD prepared with use of Ni-catalyst, S BET was about 400 m 2 /g, while for the same polymer obtained over Pd-catalyst it was more than 700 m 2 /g (Table 3). Furthermore, the nature of a catalyst also governs the pore size distribution. The polyDNBD prepared on Ni-catalyst is a mesoporous material with the dominant pore size of 3.8 nm, while microporosity for this polymer was not found according to t-plot. At the same time, all polymers from NBD or its oligomers prepared in the presence of Pd-catalyst are microporous materials. The true micropore volume and micropore area were estimated by t-plot and the obtained results are presented in Table 3. Based on these data it could be concluded that addition polymers from NBD and its oligomers prepared over Pd-catalyst also have the developed external surface area (Table 3). It is interesting that metathesis polyDNBD, which is an isomer of addition polyDNBD, exhibited extremely low value of BET surface area. This difference in the properties of two isomeric polymers might be explained by various rigidity of polymer main chains. Thus, it was shown that addition polynorbornenes possess more rigid main chains than the similar metathesis polymers [31,32]. So, in the case of addition polymers, a looser packing of polymer chains should be formed due to more rigid main chains, which could not be packed densely. Micropore size distribution was calculated using Horvath-Kawazoe method. For these estimations, the model of slit-shape pores was used. It is interesting that for polyDNBD prepared using Pd-catalyst the bimodal micropore size distribution is observed (Figure 7). The maxima are at 0.8 nm (main) and 1.1 nm. After hydrogenation, the intensity of the maximum at 1.1 nm gets higher. Micropore size distribution was calculated using Horvath-Kawazoe method. For these estimations, the model of slit-shape pores was used. It is interesting that for polyDNBD prepared using Pd-catalyst the bimodal micropore size distribution is observed (Figure 7). The maxima are at 0.8 nm (main) and 1.1 nm. After hydrogenation, the intensity of the maximum at 1.1 nm gets higher. At the same time, the micropore size distribution for polyTNBD is more narrow and unimodal, with a mean size of 0.8 nm ( Figure 7D). Therefore, it is possible to tune the average micropore size by the choice of the nature of norbornene type monomer. The unimodal and narrow size distribution obtained for polyTNBD can be promising for membrane gas separation or its application in gas storage and polyTNBD may be used as a filler for the composite membranes. The study of the porous structure of the prepared polymers by CO2 adsorption revealed that these polymers possess surface areas in the range of 200-403 m 2 /g ( Table 4). The shape of adsorption curves is I-type, indicating monomolecular adsorption (Figure 8). In the case of polymers prepared using the Pd-catalyst, a significant adsorption was observed at low CO2 pressure (at the beginning of the curves), while for polyDNBD obtained using a Ni-catalytic system, this was not found. The evaluation of the micropore size distribution showed the presence of a very narrow unimodal distribution with the mean pore size of 0.8 nm (Figure 9).
The synthesized polymers gave good CO2 uptake at 273 K, which varies from 1.2 to 1.9 mmol/g ( Table 4). The highest value of CO2 uptake was achieved for polyTNBD, exhibiting also the highest BET surface area from N2 adsorption.  The study of the porous structure of the prepared polymers by CO 2 adsorption revealed that these polymers possess surface areas in the range of 200-403 m 2 /g ( Table 4). The shape of adsorption curves is I-type, indicating monomolecular adsorption (Figure 8). In the case of polymers prepared using the Pd-catalyst, a significant adsorption was observed at low CO 2 pressure (at the beginning of the curves), while for polyDNBD obtained using a Ni-catalytic system, this was not found. The evaluation of the micropore size distribution showed the presence of a very narrow unimodal distribution with the mean pore size of 0.8 nm (Figure 9).
The synthesized polymers gave good CO 2 uptake at 273 K, which varies from 1.2 to 1.9 mmol/g ( Table 4). The highest value of CO 2 uptake was achieved for polyTNBD, exhibiting also the highest BET surface area from N 2 adsorption.

Conclusions
Addition and metathesis homopolymerization of NBD and its oligomers were studied as a way to generate new porous polymer materials. It was shown for the first time that metathesis polymerization of these monomers led to polymers with a low BET surface area, while addition polymerization gave porous materials possessing large BET surface area (up to 970 m 2 /g). The

Conclusions
Addition and metathesis homopolymerization of NBD and its oligomers were studied as a way to generate new porous polymer materials. It was shown for the first time that metathesis polymerization of these monomers led to polymers with a low BET surface area, while addition polymerization gave porous materials possessing large BET surface area (up to 970 m 2 /g). The porosity of the addition polymers formed based on NBD and its oligomers can be tuned by the catalyst choice, the nature of monomer and the post-polymerization modification. Therefore, it was

Conclusions
Addition and metathesis homopolymerization of NBD and its oligomers were studied as a way to generate new porous polymer materials. It was shown for the first time that metathesis polymerization of these monomers led to polymers with a low BET surface area, while addition polymerization gave porous materials possessing large BET surface area (up to 970 m 2 /g). The porosity of the addition polymers formed based on NBD and its oligomers can be tuned by the catalyst choice, the nature of monomer and the post-polymerization modification. Therefore, it was found that the Ni-catalytic system gave mesoporous polymers, while addition polymers prepared on the Pd-catalyst were microporous. Specific surface area of polymers increased when the size of the bifunctional monomer became larger. The largest BET surface area as high as 970 m 2 /g was reached in the case of addition polymer from the trimer of norbornadiene-2,5 and this value is the largest among BET surface area values reported for polynorbornenes so far.
Supplementary Materials: The following ( Figures S1-S4) are available online at http://www.mdpi.com/2073-4360/10/12/1382/s1, Figure S1: IR spectra of homopolymers based on NBD and its oligomers, Figure S2: IR spectra of ozonated homopolymers based on NBD and its oligomers, Figure S3: IR spectra of oxidized and initial polyDNBD (Pd-catalyst). The oxidation was performed by heating of the sample in air for 30 min, Figure S4: Nitrogen adsorption-desorption isotherms of homopolymers from NBD and its oligomers.