Nitrile Groups as Hydrogen-Bond Acceptors in a Donor-Rich Hydrogen-Bonding Network. Supplementary Information

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Nitrile Groups as Hydrogen-Bond Acceptors in a Donor-Rich Hydrogen-Bonding Network David R. Turner,* a Alison J. Edwards b and Ross O. Piltz b Supplementary Information Section 1 Structural Parameters and Diagrams Table S1 Hydrogen-bonding interactions in (NH 2 ) 3 C cdm from neutron data (c.f. Table 1, main manuscript). Interaction D-H (Å) H A (Å) D A (Å) D-H A ( ) N(1) O(1)#1 1.014(4) 1.882(4) 2.889(2) 171.6(3) N(1) N(2)#2 0.993(4) 2.445(5) 3.131(2) 125.8(3) N(4) O(1)#3 1.008(5) 1.998(5) 2.877(2) 144.1(4) N(4) N(2) 0.998(4) 2.242(5) 3.122(2) 146.2(3) N(5) O(1)#3 1.007(4) 1.981(4) 2.881(2) 147.5(3) N(5) N(3)#4 1.004(4) 2.291(4) 3.155(2) 143.5(3) N(6) N(2) 1.003(4) 2.147(4) 3.054(2) 149.5(3) N(6) N(3)#4 1.007(4) 2.021(4) 2.962(2) 154.5(4) a Symmetry equivalents used; #1, -x, -y+1, -z; #2, -x+1, -y+1, -z; #3, 1+x, y-1, z; #4, 1-x, y-3/2, 1/2-z. Table S2 Hydrogen-bonding interactions in (NH 2 ) 3 C cdm from X-ray data. Interaction D-H (Å) H A (Å) D A (Å) D-H A ( ) N(1) O(1)#1 0.870(16) 2.032(16) 2.8967(13) 172.6(14) N(1) N(2)#2 0.878(16) 2.520(16) 3.1243(15) 126.6(13) N(4) O(1)#3 0.886(17) 2.101(17) 2.8750(14) 145.5(14) N(4) N(2) 0.887(17) 2.334(18) 3.1231(15) 148.2(15) N(5) O(1)#3 0.869(18) 2.090(18) 2.8798(15) 150.7(14) N(5) N(3)#4 0.896(17) 2.360(17) 3.1526(16) 147.5(14) N(6) N(2) 0.899(17) 2.240(17) 3.0603(15) 151.5(15) N(6) N(3)#4 0.894(19) 2.124(19) 2.9607(15) 155.6(15) a Symmetry equivalents used as per Table 1 Table S3: Deviations from least-squares mean plane of C5-N4-N5-N6 (the guanidinium cation) in ((NH 2 ) 3 C)(cdm) from neutron diffraction data. C5-0.0155 (0.0013) N4 0.0052 (0.0004) N5 0.0051 (0.0004) N6 0.0052 (0.0004) H4A -0.0515 (0.0049) H4B -0.0761 (0.0050) H5A -0.1541 (0.0048) H5B -0.1694 (0.0044) H6A -0.0235 (0.0047) H6B -0.0816 (0.0049)

Table S4: Deviations from least-squares mean plane of non-hydrogen atoms in the cdm anion from neutron diffraction data. C1 0.0453 (0.0015) C2 0.0041 (0.0013) C3 0.0238 (0.0013) C4 0.0035 (0.0014) N1 0.0183 (0.0011) N2-0.0359 (0.0010) N3-0.0163 (0.0009) O1-0.0429 (0.0014) H1A 0.0226 (0.0040) H1B 0.1347 (0.0050) Figure S1: Crystal packing of ((NH 2 ) 3 C)(cdm) viewed along the a-axis.

Figure S2: Crystal packing of ((NH 2 ) 3 C)(cdm) viewed along the b-axis. Figure S3: Crystal packing of ((NH 2 ) 3 C)(cdm) viewed along the c-axis.

Section 2 - Cambridge Structural Database Search Details and Results Search Details Searches were carried out using CSD Version 5.33 (November 2011) + 1 update (Feb 2012). In all cases the search parameters required the H N contacts to be within the sum of the vdw radii (N + H = 2.750 Å). For searches containing 6-membered chelating rings with two NH donor groups it was specified that there must be a non-metal atom between the two nitrogen atoms in order to remove coordinated en/pn from results. Metal-coordinated nitriles (i.e. CN - ligands) were excluded from all searches. No filters were placed on the bond orders within the chelating donor group. Results from all searches were limited to those entries that had 3D coordinates determined, R factors <= 0.1 and no disorder or errors. All X-H distances were normalised to neutron distances. General NH Nitrile Interactions An initial search was conducted to examine the spread of distances and geometries of NH N interactions to organic nitrile groups regardless of what supramolecular motifs they are involved in. Plots shown in Figure S4 show the distribution of NH N distances that were found for the entire data sample as well as for two sub-categories, SCN groups and acetonitrile molecules. These two sub-classes are very prevalent in the database and were examined briefly to determine whether the type of species that the nitrile group is part of (and therefore the electronic nature of the nitrile group) has any major change on the length of the hydrogen-bonding interaction. The mean NH N distance for all interactions is 2.211 Å with the mean observed for SCN being slightly shorter (2.116 Å) and that for MeCN being slightly longer (2.223 Å) as would be expected. For the purposes of our intended study (the asymmetry of R (6) motifs) no distinction will be made between these sub-classes of nitrile acceptor groups. The NH Nitrile dataset was also analysed for any relationship between the NH N distance and the angle of approach, in terms of both the NH N and C N H angles. These distance vs. angle scatter plots (Figure S5) show a definite preference for both the NH N and C N H angles to approach linearity from the clustering of points. Whilst this is generally expected for the NH N interaction it is very interesting to note this trend for the C N H angle which supports the work of Le Questel showing that the minimum electrostatic potential lies at, or near, the lone pair of the sp nitrogen atom (see main paper). In addition to this clustering both plots demonstrate a general trend that longer NH N distances are associated with more acute angles with the trend being more pronounced for NH N angles than C N H angles.

Figure S4: Histograms of NH N hydrogen bonding distances to organic nitrile groups using normalised N-H distances for all nitrile groups (top left), SCN (top right) and MeCN (bottom left). The data show that there are not vast differences in the distribution depending on the type of nitrile.

Electronic Supplementary Material (ESI) for CrystEngComm Figure S5: Scatter plots for N H vs N-H N (left) and N H vs H N C (right) for all NH N interactions to organic nitrile groups. (6) Interactions to Nitrile Groups A search was conducted using the criteria outlined above to explore the geometrical preferences, if any, associated with R (6) hydrogen-bonding motifs involving nitrile as the donor group and two N-H units as the donors. The search resulted in 32 hits one of which, CSD code ABGTCU, was excluded due to nonsensical angles around the sp2 nitrogen donor atoms. Geometric parameters were extracted from the search results according to Figure S6. These are tabulated in Table S4 with θ1 set as the largest angle. Figure S6: Definition of terms used to describe the geometry of hydrogen-bonding interactions in the R (6) motif around a nitrile group (c.f. Fig. 4, main paper)

Table S4: Geometric parameters for... Note that for (d 2 d 1 ) positive values are instances where the more acute θ angle has a longer associated N H distance. CSD RefCode θ 1 θ 2 d 1 d 2 θ 1 θ 2 d 2 d 1 FANXIC 149.391 149.113 2.721 2.084 0.278-0.637 BAFSOQ 151.324 149.772 2.375 2.367 1.552-0.008 MAHVAS 154.281 151.504 1.953 2.539 2.777 0.586 CYAMPD03 136.663 124.781 2.198 2.078 11.882-0.12 WEPFON 150.381 137.158 2.227 1.847 13.223-0.38 UJETAE 135.148 121.773 2.232 1.965 13.375-0.267 GAFFAV 154.982 141.359 1.955 2.342 13.623 0.387 YOWDAQ 125.917 112.043 2.169 2.231 13.874 0.062 RENTIN 159.249 144.222 2.082 2.464 15.027 0.382 FOWMEJ 99.804 84.622 2.315 2.437 15.182 0.122 RENTIN01 159.717 144.434 2.082 2.456 15.283 0.374 GAFFAV01 155.957 139.812 1.955 2.365 16.145 0.41 GAFFAV01 157.568 141.13 2.004 2.308 16.438 0.304 GAFFAV 160.285 137.495 2.008 2.299 22.79 0.291 QIXJAJ 152.176 128.175 2.379 2.275 24.001-0.104 DIDRAJ 163.365 136.927 2.055 2.503 26.438 0.448 GITZUF 166.301 136.312 1.875 2.472 29.989 0.597 REMWOV 134.757 102.009 1.897 1.992 32.748 0.095 HIFZUR 134.598 100.199 1.884 1.998 34.399 0.114 TCAGTU 107.586 70.762 2.124 2.632 36.824 0.508 TCAGTU02 108.37 69.067 2.084 2.618 39.303 0.534 DAWDAH 167.667 127.6 1.948 2.241 40.067 0.293 CEKGOP 126.022 85.749 2.104 2.715 40.273 0.611 ZUZXIB 150.429 109.002 1.977 2.587 41.427 0.61 COFRIY10 158.162 116.678 1.984 2.599 41.484 0.615 EMEMUF 168.536 122.755 1.846 2.205 45.781 0.359 COFROE10 163.635 117.279 2.179 2.694 46.356 0.515 PEFGIR 156.499 109.069 2.119 2.692 47.43 0.573 MAHVAS 154.281 105.891 1.953 2.742 48.39 0.789 HOXVIA 151.806 96.908 2.318 2.464 54.898 0.146 REXZUP 163.005 107.003 2.291 2.056 56.002-0.235 WUNNUP 142.845 86.148 2.001 2.452 56.697 0.451 TUFDIH 155.38 98.481 2.046 2.413 56.899 0.367 LORLAG 164.431 107.271 1.998 2.253 57.16 0.255 The results in Table S4, in which θ 1 is set as the largest angle, means that if d2-d1 is a positive value then the longer H N distance is associated with the more acute H N C angle in that R (6) interaction. Out of the 33 results that are listed only 6 go against this expectations with one of these showing a difference of only 0.008 Å between the two H N contacts.