In order to perform time­resolved photocrystallographic studies on molecules embedded within a periodic host framework,1,2we have synthesized a number of new, supramolecular host–guest complexes.3C­Methylcalix[4]resorcinarene (CMCR) is a particularly suitable building block for such solids, as, together with ‘pillar’ molecules such as 4,4′­bipyridine (bipy), it can form solids with large cavities capable of including organic or inorganic guests.4,5In a previous communication we reported a two­dimensional, brick­like framework incorporating decamethylruthenocene (DMR), with CMCR in a flattened cone (C2v) conformation, not previously observed for this molecule.3We describe here three solids – CMCR·3bipy1,CMCR·3bipy·benzophenone·2H2O2, and CMCR·3bpe3[bpe⊕=⊕trans-bis(4­pyridyl)ethylene] – with a new framework in which the CMCR molecules have the (C2h) chair conformation.6The rings located on the local two­fold axis bisecting the molecule are coplanar, while the other two rings are almost perpendicular to the plane containing the first two rings with a dihedral angle of 94.36(2)°. Although this conformation has been observed for other calix[4]resorcinarene derivatives,7–10it has not been reported previously for CMCR.3,11The formation of at least three conformations of one calix[4]resorcinarene demonstrates the flexibility of the molecularframe, together with the dependence of the conformation upon the templating molecules and also upon the specifics of the crystallization process.The new solids are synthesized by hydrothermal methods,12used widely in the preparation of quartz, zeolites and inorganic–organic hybrid open frameworks but less often for the synthesis of supramolecular organic systems.13Low temperature X­ray diffraction analysis (Table 1) shows that1consists of a three­dimensional, hydrogen­bonded network. The four methyl groups of CMCR are in axial positions and have the rctt (reference–cis–trans–trans) arrangement of theC2hchair conformation, (Fig. 1) rather than the previously reported crown­shaped (C4v)14or flattened cone (C2v) rccc conformations,3,15the CMCR molecules being located on a crystallographic center of symmetry.The CMCR chair conformation as observed in1.Crystal data for1–3,,123All data were collected atT⊕=⊕90(1) K using a Bruker SMART1000 CCD with MoKα radiation (λ⊕=⊕0.71073 Å).Intensities were reduced using the SAINT program; structures were solved by direct methods and refined by a full­matrix, least squares technique based onF 2using SHELXL97.Clickherefor full crystallographic data (CCDC 158837–158839).Empirical formulaC62H56N6O8C75H70N6O11C68H62N6O8Crystal dimensions/mm0.30⊕×⊕0.18⊕×⊕0.100.32⊕×⊕0.12⊕×⊕0.100.40⊕×⊕0.32⊕×⊕0.06M1013.131231.371091.24Crystal systemTriclinicTriclinicTriclinicSpace groupP1&cmb.macr;P1P1&cmb.macr;a/Å9.8060(6)9.9541(14)10.7187(4)b/Å10.8427(6)11.5239(16)11.1242(4)c/Å13.0429(8)14.3145(14)13.1204(5)α/°74.672(2)82.333(5)110.452(1)β/°73.633(2)74.456(4)105.252(1)γ/°89.016(2)80.836(3)96.896(1)U/Å31280.78(13)1554.6(3)1374.76(9)Z111Dc/Mg m−31.3141.3151.318μ(Mo­Kα)/mm−10.0880.0890.087F(000)534650576GoF0.9510.8391.011Number of reflections (unique)12 555 (6214)15 198 (12 553)9578 (6202)Rint0.05340.04740.0318Number of observed reflections [I⊕>⊕2σ(I)]399063514282Number of refined parameters4561011495R10.05500.05320.0483wR20.13780.09560.1220Adjacent CMCR molecules are connected into infinite columns parallel to the crystallographic [010] direction through two, center­of­symmetry­related, phenoxyl O–H⋯O hydrogen bonds per molecular pair [O1⋯O3a⊕=⊕2.7071(7) Å, O1–H1⋯O3a⊕=⊕163.5(11)°;a⊕=⊕−x⊕+⊕1, −y⊕+⊕2, −z⊕+⊕1]. As shown inFig. 2, O–H⋯N hydrogen bonds between the axial phenoxyl groups and bipyridine molecules link the columns into stair­like sheets parallel to the (011) plane [O4⋯N2⊕=⊕2.7529(9) Å, O4–H4⋯N2⊕=⊕176.2(11)°; O3⋯N1b⊕=⊕2.6712(9) Å,O3–H3⋯N1b⊕=⊕167.7(12)°;b⊕=⊕−x, −y⊕+⊕2, −z]. The sheets are connected with each other by a second set of bipyridyl molecules through O–H⋯N hydrogen bonds giving rise to a three­dimensional network [O2⋯N3c⊕=⊕2.8885(10) Å, O2–H2⋯N3c⊕=⊕174.0(8)°;c⊕=⊕x,y⊕+⊕1,z] (Fig. 3).The stepped sheet of1, consisting of hydrogen­bonded CMCR and bipyridine molecules, (a) viewed along the [100] direction, (b) viewed along [010]. Click image orhereto access a 3D representation.The three­dimensional network of1. One sheet is shown. Bipyridine molecules connecting the sheets are shown in yellow. Click image orhereto access a 3D representation.Three different kinds of host structures formed by CMCR and bipyridine which are capable of including guest molecules have been described in the literature: a 0D carcerand­like capsule;16a 1D wave­like polymer;5and a 2D brick­wall­like sheet.3The stepped network can similarly accommodate guest molecules, as demonstrated by the structure of CMCR·3bipy·benzophenone·2H2O2, in which CMCR also adopts a chair conformation. As shown inFig. 4, in crystals of2the CMCR molecules are again linked into hydrogen­bonded columns, oriented parallel to the [100] direction, with water molecules interspersed between the CMCRs being part of the columns. The columns are connected into stepped sheets by bipyridine molecules, asin1, with large spaces remaining between dimeric bipyridine units. A second set of bipyridine molecules connects the sheets into a 3D network similar to that of1such that infinite channels are formed by adjacent cavities in successive sheets, the guest benzophenone molecules being located within the channels (Fig. 4).The three­dimensional, hydrogen­bonded framework of2, formed by CMCR, bipyridine and water molecules, showing the guest benzophenone molecules. The bipyridine molecules linking the stepped sheets are shown in yellow. Click image orhereto access a 3D representation.The shape of the guest molecules is affected by the host matrix: the twist angles between the C(C&z.dbd6;O)C plane and the two phenyl ring planes of benzophenone are 29.3(2) and 16.7(3)°, significantly different from those in neat benzophenone crystals (α form: 31.0 and 28.7°,1730.8 and 30.0°;18β form: 30.8 and 46.8°19). The carbonyl oxygen atom of benzophenone forms a hydrogen bond with one of the water molecules.In photochemical studies of host–guest complexes of benzil and decamethylruthenocene we have found considerable differences between triplet state lifetimes of the same guest species within different host frameworks, illustrating the effect of the environment upon the photochemical properties.20(The relation between the molecular conformation of benzophenone and the triplet state lifetimes is to be explored in subsequent studies.) As expected, an appreciable dilution of the photoactive guest is achieved in the host–guest crystal2(1.07vs.6.64 mol dm−3in the neat solid).17When bipyridine is replaced bytrans-bis(4­pyridyl)ethylene (bpe) in the reaction mixture used to prepare1, a third solid, CMCR·3bpe3, is formed. It is isostructural with1, with CMCR again in the chair conformation, and has a stepped 3D framework (Fig. 5).The two­dimensional stepped sheet of3. Click image orhereto access a 3D representation.In summary, the chair conformation for CMCR has been observed for the first time in several different phases prepared by hydrothermal synthesis, by which a novel, three­dimensional framework, capable of including guest molecules, has been synthesized.