Supplementary Figure 1. Large-area SEM images of rhombic rod foldectures (F1) deposited on Si substrate in (a) an in-plane magnetic field and (b) an
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1 Supplementary Figure 1. Large-area SEM images of rhombic rod foldectures (F1) deposited on Si substrate in (a) an in-plane magnetic field and (b) an out-of-plane magnetic field. Scale bars: 10 m. 1
2 Supplementary Figure 2. Large-area SEM images of rectangular plate foldectures (F2) deposited on Si substrate in (a) an in-plane magnetic field and (b) an out-of-plane magnetic field. Scale bars: 10 m. 2
3 Supplementary Figure 3. (a) The final Rietveld plot for foldectures F2. The observed (red cross) intensities were superimposed on the calculated (green line) intensities. The difference profile was plotted as magenta line. The 2 range higher than 25 was magnified 10 times for clarity of high-angle data. (b) Transmission electron microscopy image of a F2 and (inset) corresponding selected area electron diffraction pattern (from a view along [100] zone axis). Crystallographic c and b axes lie along the major and minor axes of the rectangular plate, respectively. (c) Molecular structure of foldecture F2 in the unit cell. 3
4 Supplementary Figure 4. Calculated diamagnetic susceptibility tensors in crystal structures of (a) F1 and (b) F2. Total diamagnetic susceptibility was estimated by linear combination of each susceptibility tensor for four peptide molecules, indicated by different colours (magenta, azure, green, and yellow). 4
5 Supplementary Figure 5. Molecular packing structures of (a) F1 and (b) F2 from views along the a, c axes, respectively. Colored arrows indicate the direction of the helical axis (N termini to C termini). 5
6 Supplementary Figure 6. Contributions of (a) the peptides with methyl ester (BocNH- ACPC 8 -OMe) and (b) C-terminal benzene groups to the total diamagnetic susceptibility in the crystal structure of F2. 6
7 Supplementary Figure 7. (a) Angle ( ) made from the helical axis (gray) of model peptides and easy magnetization axis (yellow) obtained from DFT calculation. (b) Table of the maximum diamagnetic anisotropic susceptibilities and estimated angles ( ) for model 12- helical trans-acpc homooligomers (BocNH-ACPC n -OR, n = 6, 8, 10, 12) with various C- terminal functional groups (methyl, benzyl, and naphthalene-2-ylmethyl). Arrows indicate direction of the easy magnetization axis of each peptide (black: methyl, red: benzyl, blue: naphthalene-2-ylmethyl). 7
8 Supplementary Figure 8. (a) Top view and (b) side view of the experimental configuration for the optical microscope equipped with homebuilt rotating magnetic field device. 8
9 Supplementary Figure 9. (a,b) Snapshots taken from optical microscopy videos and schematic representations showing the foldectures F2 suspended in water under rotating magnetic field. Arrows indicate the direction of magnetic field. Scale bars: 10 m. 9
10 Supplementary Figure 10. (a) Optical microscopy image showing the aligned foldectures F1 inside the hydrogel container. Scale bar: 10 m. Arrow indicates the direction of applied magnetic field during photopolymerization process. (b) Photograph of rhombus-shaped macroscopic hydrogel container floating on the water with rotating magnetic field device. Horizontal magnetic field (B) is generated between the nodes of cylindrical magnets. Scale bar: 5 mm. 10
11 Supplementary Tables Supplementary Table 1. The powder diffraction experimental details of F2. Crystal data Chemical formula C 60 N 8 O 11 M r Cell setting, space group Orthorhombic, P Temperature (K) Room temperature a, b, c (Å) (14), (5), (18) V(Å 3 ) (16) Z 4 Radiation type Synchrotron Specimen form, color Flat type (particle morphology: thin plate type powder),white Specimen preparation temperature Room temperature Data Collection Diffractometer Data collection method 2 ( ) 9B HRPD, PAL, Pohang, Republic of Korea Specimen mounting: silicon non-reflection holder; mode: Reflection mode, Bragg- Brentano geometry; scan method: step, fixed 2 min =4.5, 2 max=60, increment=0.005 Refinement Refinement on Observed intensities Preferred orientation correction March-Dollase model, for (100), P MD = R Factors and goodness-of-fit R p =0.0597, R wp =0.0772, R exp =0.0332, S=2.33 Wavelength of incident radiation (Å) Excluded region(s) None Profile function Pseudo-voigt No. of parameters 240 H-atom treatment Omitted during the whole process for clarity 11
12 Supplementary Table 2. Atomic coordination table of F2. Name Atom type x y Z Occupancy Uiso Multiplicity C1 C (6) (6) (14) (7) 4 C2 C (6) (5) (17) (7) 4 C3 C (5) (5) (18) (7) 4 C4 C (32) (27) (9) (7) 4 O5 O (26) (24) (23) (7) 4 C6 C (25) (19) (15) (7) 4 O7 O (34) (31) (22) (7) 4 N8 N (31) (25) (12) (7) 4 C9 C (33) (28) (7) (7) 4 C10 C (4) (7) (11) (7) 4 C11 C (5) (9) (17) (7) 4 C12 C (4) (6) (13) (7) 4 C13 C (32) (26) (7) (7) 4 C14 C (4) (17) (6) (7) 4 O15 O (4) (29) (12) (7) 4 N16 N (4) (26) (8) (7) 4 C17 C (34) (29) (7) (7) 4 C18 C (5) (5) (12) (7) 4 C19 C (5) (9) (14) (7) 4 C20 C (4) (6) (11) (7) 4 C21 C (33) (25) (7) (7) 4 C22 C (4) (17) (6) (7) 4 O23 O (4) (30) (11) (7) 4 N24 N (4) (23) (9) (7) 4 C25 C (32) (27) (8) (7) 4 C26 C (4) (6) (13) (7) 4 C27 C (5) (7) (15) (7) 4 C28 C (4) (5) (11) (7) 4 C29 C (32) (24) (8) (7) 4 C30 C (27) (17) (11) (7) 4 O31 O (35) (29) (21) (7) 4 N32 N (34) (24) (13) (7) 4 C33 C (32) (28) (8) (7) 4 C34 C (4) (7) (12) (7) 4 C35 C (4) (8) (18) (7) 4 C36 C (4) (5) (14) (7) 4 C37 C (30) (26) (8) (7) 4 12
13 C38 C (28) (18) (10) (7) 4 O39 O (4) (29) (18) (7) 4 N40 N (33) (25) (12) (7) 4 C41 C (32) (28) (8) (7) 4 C42 C (4) (4) (12) (7) 4 C43 C (5) (9) (15) (7) 4 C44 C (4) (6) (13) (7) 4 C45 C (31) (25) (7) (7) 4 C46 C (4) (18) (6) (7) 4 O47 O (4) (30) (11) (7) 4 N48 N (4) (23) (9) (7) 4 C49 C (4) (25) (7) (7) 4 C50 C (5) (4) (11) (7) 4 C51 C (5) (6) (15) (7) 4 C52 C (5) (4) (11) (7) 4 C53 C (4) (24) (7) (7) 4 C54 C (4) (18) (6) (7) 4 O55 O (4) (31) (12) (7) 4 N56 N (4) (26) (8) (7) 4 C57 C (33) (31) (7) (7) 4 C58 C (4) (7) (13) (7) 4 C59 C (5) (8) (16) (7) 4 C60 C (4) (6) (11) (7) 4 C61 C (31) (29) (7) (7) 4 C62 C (26) (23) (7) (7) 4 O63 O (4) (4) (12) (7) 4 N64 N (31) (28) (11) (7) 4 C65 C (31) (25) (9) (7) 4 C66 C (4) (4) (15) (7) 4 C67 C (6) (6) (16) (7) 4 C68 C (5) (5) (11) (7) 4 C69 C (4) (24) (8) (7) 4 C70 C (33) (19) (7) (7) 4 O71 O (4) (4) (11) (7) 4 O72 O (30) (25) (12) (7) 4 C73 C (4) (29) (11) (7) 4 C74 C (20) (24) (5) (7) 4 C75 C (19) (26) (4) (7) 4 C76 C (27) (25) (8) (7) 4 13
14 C77 C (30) (21) (7) (7) 4 C78 C (29) (15) (6) (7) 4 C79 C (29) (27) (7) (7) 4 14
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