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Table 3 Donor–acceptor distances, hydrogen bond lengths, and angles in SC 1

From: Synthesis, crystal structural description, DNA binding, molecular docking, and anticancer evaluation of the novel platinum(IV) supramolecular complex

D-AH

d(D-H)/Å

d(H-A)/Å

d(D-A)/Å

D-H-A/°

C3–H3Cl3a

0.95

2.88

3.640(5)

137.4

C3–H3Cl4b

0.95

2.85

3.507(5)

126.8

C4–H4Cl2a

0.95

2.78

3.694(6)

162.1

C6–H6Cl4c

0.95

2.74

3.364(5)

124.0

C7–H7Cl4c

0.95

2.90

3.664(6)

138.6

C9–H9Cl4d

0.95

2.70

3.644(6)

172.4

C10–H10Cl1

0.95

2.72

3.314(6)

121.2

C3–H3N1

0.95

2.64

3.174(6)

116.2

  1. a1/2-X,−1/2 + Y,1/2-Z
  2. b+ X,1-Y,−1/2 + Z
  3. c1-X, + Y,1/2-Z
  4. d1/2-X,1/2 + Y,1/2-Z